A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv695232



Internal ID15085198
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:55622443..55664115hg38UCSC Ensembl
Innerchr16:55656355..55698027hg19UCSC Ensembl
Innerchr16:54213856..54255528hg18UCSC Ensembl
Innerchr16:54213856..54255528hg17UCSC Ensembl
Cytoband16q12.2
Allele length
AssemblyAllele length
hg3841673
hg1941673
hg1841673
hg1741673
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517827
Supporting Variants
Samples
Known GenesSLC6A2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv695232
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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