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nsv1159738

  • Variant Calls:1
  • 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: 526 SVs from 41 studies. See in: genome view    
Remapped(Score: Perfect):77,549,051-77,549,051Question Mark
Overlapping variant regions from other studies: 534 SVs from 43 studies. See in: genome view    
Remapped(Score: Perfect):77,549,534-77,549,534Question Mark
Overlapping variant regions from other studies: 526 SVs from 41 studies. See in: genome view    
Submitted genomic75,261,007-75,261,007Question Mark
Overlapping variant regions from other studies: 534 SVs from 43 studies. See in: genome view    
Submitted genomic75,261,490-75,261,490Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStopstrand
nsv1159738RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000018.10Chr1877,549,05177,549,051not reported
nsv1159738RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000018.10Chr1877,549,53477,549,534not reported
nsv1159738Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000018.9Chr1875,261,00775,261,007not reported
nsv1159738Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000018.9Chr1875,261,49075,261,490not reported

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysisOther Calls in this Sample and Study
nssv4024919intrachromosomal translocationKWS1SequencingRead depth and paired-end mapping22,470

Variant Call Placement Information

Variant Call IDPlacement TypeScoreAssemblyReciprocitySequence IDChrStartStopstrand
nssv4024919RemappedPerfectGRCh38.p12First PassNC_000018.10Chr1877,549,05177,549,051not reported
nssv4024919RemappedPerfectGRCh38.p12First PassNC_000018.10Chr1877,549,53477,549,534not reported
nssv4024919Submitted genomicGRCh37 (hg19)NC_000018.9Chr1875,261,00775,261,007not reported
nssv4024919Submitted genomicGRCh37 (hg19)NC_000018.9Chr1875,261,49075,261,490not reported

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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