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nsv4431138

  • Variant Calls:6
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 108 SVs from 22 studies. See in: genome view    
Remapped(Score: Perfect):106,878,541-106,878,541Question Mark
Overlapping variant regions from other studies: 130 SVs from 31 studies. See in: genome view    
Remapped(Score: Perfect):120,131,588-120,131,588Question Mark
Overlapping variant regions from other studies: 159 SVs from 24 studies. See in: genome view    
Remapped(Score: Perfect):143,373,781-143,373,781Question Mark
Overlapping variant regions from other studies: 417 SVs from 67 studies. See in: genome view    
Remapped(Score: Perfect):143,845,117-143,845,117Question Mark
Overlapping variant regions from other studies: 169 SVs from 26 studies. See in: genome view    
Remapped(Score: Perfect):145,141,408-145,141,408Question Mark
Overlapping variant regions from other studies: 113 SVs from 29 studies. See in: genome view    
Remapped(Score: Perfect):94,354,241-94,354,241Question Mark
Overlapping variant regions from other studies: 206 SVs from 21 studies. See in: genome view    
Remapped(Score: Perfect):113,632,611-113,632,611Question Mark
Overlapping variant regions from other studies: 256 SVs from 35 studies. See in: genome view    
Remapped(Score: Perfect):114,153,921-114,153,921Question Mark
Overlapping variant regions from other studies: 260 SVs from 36 studies. See in: genome view    
Remapped(Score: Perfect):114,309,798-114,309,798Question Mark
Overlapping variant regions from other studies: 235 SVs from 22 studies. See in: genome view    
Remapped(Score: Perfect):114,517,074-114,517,074Question Mark
Overlapping variant regions from other studies: 235 SVs from 22 studies. See in: genome view    
Remapped(Score: Perfect):114,517,076-114,517,076Question Mark
Overlapping variant regions from other studies: 243 SVs from 25 studies. See in: genome view    
Remapped(Score: Perfect):62,627,747-62,627,747Question Mark
Overlapping variant regions from other studies: 108 SVs from 22 studies. See in: genome view    
Submitted genomic106,518,986-106,518,986Question Mark
Overlapping variant regions from other studies: 130 SVs from 31 studies. See in: genome view    
Submitted genomic119,771,642-119,771,642Question Mark
Overlapping variant regions from other studies: 159 SVs from 24 studies. See in: genome view    
Submitted genomic143,070,874-143,070,874Question Mark
Overlapping variant regions from other studies: 417 SVs from 67 studies. See in: genome view    
Submitted genomic143,542,210-143,542,210Question Mark
Overlapping variant regions from other studies: 169 SVs from 26 studies. See in: genome view    
Submitted genomic144,838,501-144,838,501Question Mark
Overlapping variant regions from other studies: 113 SVs from 29 studies. See in: genome view    
Submitted genomic93,983,553-93,983,553Question Mark
Overlapping variant regions from other studies: 206 SVs from 21 studies. See in: genome view    
Submitted genomic114,644,840-114,644,840Question Mark
Overlapping variant regions from other studies: 256 SVs from 35 studies. See in: genome view    
Submitted genomic115,166,150-115,166,150Question Mark
Overlapping variant regions from other studies: 260 SVs from 36 studies. See in: genome view    
Submitted genomic115,322,027-115,322,027Question Mark
Overlapping variant regions from other studies: 235 SVs from 22 studies. See in: genome view    
Submitted genomic115,529,303-115,529,303Question Mark
Overlapping variant regions from other studies: 235 SVs from 22 studies. See in: genome view    
Submitted genomic115,529,305-115,529,305Question Mark
Overlapping variant regions from other studies: 243 SVs from 25 studies. See in: genome view    
Submitted genomic63,201,880-63,201,880Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStopstrand
nsv4431138RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000007.14Chr7106,878,541106,878,541-
nsv4431138RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000007.14Chr7120,131,588120,131,588-
nsv4431138RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000007.14Chr7143,373,781143,373,781-
nsv4431138RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000007.14Chr7143,845,117143,845,117-
nsv4431138RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000007.14Chr7145,141,408145,141,408-
nsv4431138RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000007.14Chr794,354,24194,354,241-
nsv4431138RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000008.11Chr8113,632,611113,632,611+
nsv4431138RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000008.11Chr8114,153,921114,153,921+
nsv4431138RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000008.11Chr8114,309,798114,309,798+
nsv4431138RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000008.11Chr8114,517,074114,517,074+
nsv4431138RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000008.11Chr8114,517,076114,517,076+
nsv4431138RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000013.11Chr1362,627,74762,627,747+
nsv4431138Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000007.13Chr7106,518,986106,518,986-
nsv4431138Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000007.13Chr7119,771,642119,771,642-
nsv4431138Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000007.13Chr7143,070,874143,070,874-
nsv4431138Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000007.13Chr7143,542,210143,542,210-
nsv4431138Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000007.13Chr7144,838,501144,838,501-
nsv4431138Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000007.13Chr793,983,55393,983,553-
nsv4431138Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000008.10Chr8114,644,840114,644,840+
nsv4431138Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000008.10Chr8115,166,150115,166,150+
nsv4431138Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000008.10Chr8115,322,027115,322,027+
nsv4431138Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000008.10Chr8115,529,303115,529,303+
nsv4431138Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000008.10Chr8115,529,305115,529,305+
nsv4431138Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000013.10Chr1363,201,88063,201,880+

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysisOther Calls in this Sample and Study
nssv15745548intrachromosomal translocationD15358SequencingPaired-end mapping, Sequence alignment41
nssv15745544interchromosomal translocationD15358SequencingPaired-end mapping, Sequence alignment41
nssv15745550interchromosomal translocationD15358SequencingPaired-end mapping, Sequence alignment41
nssv15745549intrachromosomal translocationD15358SequencingPaired-end mapping, Sequence alignment41
nssv15745551intrachromosomal translocationD15358SequencingPaired-end mapping, Sequence alignment41
nssv15745552intrachromosomal translocationD15358SequencingPaired-end mapping, Sequence alignment41

Variant Call Placement Information

Variant Call IDPlacement TypeScoreAssemblyReciprocitySequence IDChrStartStopstrand
nssv15745548RemappedPerfectGRCh38.p12First PassNC_000007.14Chr794,354,24194,354,241-
nssv15745544RemappedPerfectGRCh38.p12First PassNC_000007.14Chr7106,878,541106,878,541-
nssv15745550RemappedPerfectGRCh38.p12First PassNC_000007.14Chr7120,131,588120,131,588-
nssv15745549RemappedPerfectGRCh38.p12First PassNC_000007.14Chr7143,373,781143,373,781-
nssv15745549RemappedPerfectGRCh38.p12First PassNC_000007.14Chr7143,845,117143,845,117-
nssv15745548RemappedPerfectGRCh38.p12First PassNC_000007.14Chr7145,141,408145,141,408-
nssv15745551RemappedPerfectGRCh38.p12First PassNC_000008.11Chr8113,632,611113,632,611+
nssv15745552RemappedPerfectGRCh38.p12First PassNC_000008.11Chr8114,153,921114,153,921+
nssv15745550RemappedPerfectGRCh38.p12First PassNC_000008.11Chr8114,309,798114,309,798+
nssv15745552RemappedPerfectGRCh38.p12First PassNC_000008.11Chr8114,517,074114,517,074+
nssv15745551RemappedPerfectGRCh38.p12First PassNC_000008.11Chr8114,517,076114,517,076+
nssv15745544RemappedPerfectGRCh38.p12First PassNC_000013.11Chr1362,627,74762,627,747+
nssv15745548Submitted genomicGRCh37 (hg19)NC_000007.13Chr793,983,55393,983,553-
nssv15745544Submitted genomicGRCh37 (hg19)NC_000007.13Chr7106,518,986106,518,986-
nssv15745550Submitted genomicGRCh37 (hg19)NC_000007.13Chr7119,771,642119,771,642-
nssv15745549Submitted genomicGRCh37 (hg19)NC_000007.13Chr7143,070,874143,070,874-
nssv15745549Submitted genomicGRCh37 (hg19)NC_000007.13Chr7143,542,210143,542,210-
nssv15745548Submitted genomicGRCh37 (hg19)NC_000007.13Chr7144,838,501144,838,501-
nssv15745551Submitted genomicGRCh37 (hg19)NC_000008.10Chr8114,644,840114,644,840+
nssv15745552Submitted genomicGRCh37 (hg19)NC_000008.10Chr8115,166,150115,166,150+
nssv15745550Submitted genomicGRCh37 (hg19)NC_000008.10Chr8115,322,027115,322,027+
nssv15745552Submitted genomicGRCh37 (hg19)NC_000008.10Chr8115,529,303115,529,303+
nssv15745551Submitted genomicGRCh37 (hg19)NC_000008.10Chr8115,529,305115,529,305+
nssv15745544Submitted genomicGRCh37 (hg19)NC_000013.10Chr1363,201,88063,201,880+

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

No genotype data were submitted for this variant

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