A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv702919



Internal ID15092885
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:121574688..121600223hg38UCSC Ensembl
Innerchr9:124336967..124362502hg19UCSC Ensembl
Innerchr9:123376788..123402323hg18UCSC Ensembl
Innerchr9:121416521..121442056hg17UCSC Ensembl
Cytoband9q33.2
Allele length
AssemblyAllele length
hg3825536
hg1925536
hg1825536
hg1725536
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv520039
Supporting Variants
Samples
Known GenesDAB2IP
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv702919
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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