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nsv5455624

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:585

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 96 SVs from 18 studies. See in: genome view    
Submitted genomic139,275,347-139,275,931Question Mark
Overlapping variant regions from other studies: 96 SVs from 18 studies. See in: genome view    
Remapped(Score: Perfect):138,611,036-138,611,620Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5455624Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000005.10Chr5139,275,347139,275,931
nsv5455624RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000005.9Chr5138,611,036138,611,620

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16976099deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16976099Submitted genomicNC_000005.10:g.139
275347_139275931de
l
GRCh38 (hg38)NC_000005.10Chr5139,275,347139,275,931
nssv16976099RemappedPerfectNC_000005.9:g.1386
11036_138611620del
GRCh37.p13First PassNC_000005.9Chr5138,611,036138,611,620

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

Complete genotype and/or allele frequency data for this study can be found on dbVar's FTP site.

Genotype Information

Variant Call IDAllele Frequency (AF)Allele Count (AC)Allele Number (AN)
nssv16976099<0.00166404
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