A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv701495



Internal ID15438147
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:3982715..3984066hg38UCSC Ensembl
Innerchr16:4032716..4034067hg19UCSC Ensembl
Innerchr16:3972717..3974068hg18UCSC Ensembl
Innerchr16:3972717..3974068hg17UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg381352
hg191352
hg181352
hg171352
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv525374
Supporting Variants
Samples
Known GenesADCY9
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv701495
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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