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nsv5847938

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,100

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 230 SVs from 42 studies. See in: genome view    
Submitted genomic128,852,683-128,853,782Question Mark
Overlapping variant regions from other studies: 230 SVs from 42 studies. See in: genome view    
Remapped(Score: Perfect):128,492,737-128,493,836Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5847938Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000007.14Chr7128,852,683128,853,782
nsv5847938RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000007.13Chr7128,492,737128,493,836

Variant Call Information

Variant Call IDTypeMethodAnalysisCopy number
nssv17501222copy number variationSequencingSequence alignment0

Variant Call Placement Information

Variant Call IDPlacement TypeScoreAssemblyReciprocitySequence IDChrStartStop
nssv17501222Submitted genomicGRCh38 (hg38)NC_000007.14Chr7128,852,683128,853,782
nssv17501222RemappedPerfectGRCh37.p13First PassNC_000007.13Chr7128,492,737128,493,836

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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