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nsv4716316

  • 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: 165 SVs from 41 studies. See in: genome view    
Remapped(Score: Perfect):75,945,388-75,945,388Question Mark
Overlapping variant regions from other studies: 196 SVs from 46 studies. See in: genome view    
Remapped(Score: Perfect):26,222,914-26,222,914Question Mark
Overlapping variant regions from other studies: 166 SVs from 42 studies. See in: genome view    
Submitted genomic75,994,539-75,994,539Question Mark
Overlapping variant regions from other studies: 202 SVs from 47 studies. See in: genome view    
Submitted genomic26,203,550-26,203,550Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStopstrand
nsv4716316RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000003.12Chr375,945,38875,945,388-
nsv4716316RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000020.11Chr2026,222,91426,222,914-
nsv4716316Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000003.11Chr375,994,53975,994,539-
nsv4716316Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000020.10Chr2026,203,55026,203,550-

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysisCopy numberOther Calls in this Sample and Study
nssv16248580interchromosomal translocationB450SequencingPaired-end mapping14,473

Variant Call Placement Information

Variant Call IDPlacement TypeScoreAssemblyReciprocitySequence IDChrStartStopstrand
nssv16248580RemappedPerfectGRCh38.p12First PassNC_000003.12Chr375,945,38875,945,388-
nssv16248580RemappedPerfectGRCh38.p12First PassNC_000020.11Chr2026,222,91426,222,914-
nssv16248580Submitted genomicGRCh37 (hg19)NC_000003.11Chr375,994,53975,994,539-
nssv16248580Submitted genomicGRCh37 (hg19)NC_000020.10Chr2026,203,55026,203,550-

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

Genotype and/or allele frequency data can be found on dbVar's FTP site.

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