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nsv5419641

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:38,702

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 232 SVs from 43 studies. See in: genome view    
Submitted genomic44,683,179-44,721,880Question Mark
Overlapping variant regions from other studies: 232 SVs from 43 studies. See in: genome view    
Remapped(Score: Perfect):45,148,851-45,187,552Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5419641Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr144,683,17944,721,880
nsv5419641RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr145,148,85145,187,552

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16902591deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16902591Submitted genomicNC_000001.11:g.446
83179_44721880del
GRCh38 (hg38)NC_000001.11Chr144,683,17944,721,880
nssv16902591RemappedPerfectNC_000001.10:g.451
48851_45187552del
GRCh37.p13First PassNC_000001.10Chr145,148,85145,187,552

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)
nssv16902591<0.00116404
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