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nsv5443738

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:6,001

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 167 SVs from 33 studies. See in: genome view    
Submitted genomic126,689,618-126,695,618Question Mark
Overlapping variant regions from other studies: 167 SVs from 33 studies. See in: genome view    
Remapped(Score: Perfect):127,447,194-127,453,194Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5443738Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr2126,689,618126,695,618
nsv5443738RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr2127,447,194127,453,194

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16919511duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16919511Submitted genomicNC_000002.12:g.126
689618_126695618du
p
GRCh38 (hg38)NC_000002.12Chr2126,689,618126,695,618
nssv16919511RemappedPerfectNC_000002.11:g.127
447194_127453194du
p
GRCh37.p13First PassNC_000002.11Chr2127,447,194127,453,194

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)
nssv16919511<0.00166386
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