A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv698685



Internal ID15435337
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:51718140..51727831hg38UCSC Ensembl
Innerchr16:51752051..51761742hg19UCSC Ensembl
Innerchr16:50309552..50319243hg18UCSC Ensembl
Innerchr16:50309552..50319243hg17UCSC Ensembl
Cytoband16q12.1
Allele length
AssemblyAllele length
hg389692
hg199692
hg189692
hg179692
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516564
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv698685
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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