A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv696509



Internal ID15433161
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:28710507..28826603hg38UCSC Ensembl
Innerchr9:28710505..28826601hg19UCSC Ensembl
Innerchr9:28700505..28816601hg18UCSC Ensembl
Innerchr9:28700505..28816601hg17UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg38116097
hg19116097
hg18116097
hg17116097
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv519040
Supporting Variants
Samples
Known GenesLINGO2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv696509
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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