A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv705874



Internal ID15095840
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:65148052..65148655hg38UCSC Ensembl
Innerchr16:65181955..65182558hg19UCSC Ensembl
Innerchr16:63739456..63740059hg18UCSC Ensembl
Innerchr16:63739456..63740059hg17UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg38604
hg19604
hg18604
hg17604
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv522506
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv705874
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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