A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv697107



Internal ID15087073
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:64370655..64583407hg38UCSC Ensembl
Innerchr3:64356331..64569083hg19UCSC Ensembl
Innerchr3:64331371..64544123hg18UCSC Ensembl
Innerchr3:64331371..64544123hg17UCSC Ensembl
Cytoband3p14.1
Allele length
AssemblyAllele length
hg38212753
hg19212753
hg18212753
hg17212753
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv519887
Supporting Variants
Samples
Known GenesADAMTS9
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv697107
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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