A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv705192



Internal ID15441844
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:4104850..4106856hg38UCSC Ensembl
Innerchr16:4154851..4156857hg19UCSC Ensembl
Innerchr16:4094852..4096858hg18UCSC Ensembl
Innerchr16:4094852..4096858hg17UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg382007
hg192007
hg182007
hg172007
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv528573
Supporting Variants
Samples
Known GenesADCY9
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv705192
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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