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nsv5532278

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:247,804

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 947 SVs from 65 studies. See in: genome view    
Submitted genomic69,677,060-69,924,863Question Mark
Overlapping variant regions from other studies: 947 SVs from 65 studies. See in: genome view    
Remapped(Score: Perfect):69,710,963-69,958,766Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5532278Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000016.10Chr1669,677,06069,924,863
nsv5532278RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000016.9Chr1669,710,96369,958,766

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17707135duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17707135Submitted genomicNC_000016.10:g.696
77060_69924863dup
GRCh38 (hg38)NC_000016.10Chr1669,677,06069,924,863
nssv17707135RemappedPerfectNC_000016.9:g.6971
0963_69958766dup
GRCh37.p13First PassNC_000016.9Chr1669,710,96369,958,766

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)
nssv17707135<0.00116404
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