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nsv5854386

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,462

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 146 SVs from 52 studies. See in: genome view    
Submitted genomic77,175,037-77,176,498Question Mark
Overlapping variant regions from other studies: 147 SVs from 53 studies. See in: genome view    
Remapped(Score: Perfect):76,804,354-76,805,815Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5854386Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000007.14Chr777,175,03777,176,498
nsv5854386RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000007.13Chr776,804,35476,805,815

Variant Call Information

Variant Call IDTypeMethodAnalysisCopy number
nssv17503432copy number variationSequencingSequence alignment0

Variant Call Placement Information

Variant Call IDPlacement TypeScoreAssemblyReciprocitySequence IDChrStartStop
nssv17503432Submitted genomicGRCh38 (hg38)NC_000007.14Chr777,175,03777,176,498
nssv17503432RemappedPerfectGRCh37.p13First PassNC_000007.13Chr776,804,35476,805,815

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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