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nsv5530940

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:58

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 248 SVs from 44 studies. See in: genome view    
Submitted genomic17,138,974-17,139,031Question Mark
Overlapping variant regions from other studies: 248 SVs from 44 studies. See in: genome view    
Remapped(Score: Perfect):17,232,831-17,232,888Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5530940Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000016.10Chr1617,138,97417,139,031
nsv5530940RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000016.9Chr1617,232,83117,232,888

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17704667duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17704667Submitted genomicNC_000016.10:g.171
38974_17139031dup
GRCh38 (hg38)NC_000016.10Chr1617,138,97417,139,031
nssv17704667RemappedPerfectNC_000016.9:g.1723
2831_17232888dup
GRCh37.p13First PassNC_000016.9Chr1617,232,83117,232,888

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)
nssv17704667<0.00116404
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