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nsv5551957

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:94

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 88 SVs from 20 studies. See in: genome view    
Submitted genomic41,779,142-41,779,235Question Mark
Overlapping variant regions from other studies: 88 SVs from 20 studies. See in: genome view    
Remapped(Score: Perfect):42,175,146-42,175,239Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5551957Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000022.11Chr2241,779,14241,779,235
nsv5551957RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000022.10Chr2242,175,14642,175,239

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17729175deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17729175Submitted genomicNC_000022.11:g.417
79142_41779235del
GRCh38 (hg38)NC_000022.11Chr2241,779,14241,779,235
nssv17729175RemappedPerfectNC_000022.10:g.421
75146_42175239del
GRCh37.p13First PassNC_000022.10Chr2242,175,14642,175,239

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)
nssv17729175<0.00126404
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