A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv668433



Internal ID15405085
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:2691186..2790307hg38UCSC Ensembl
Innerchr9:2691186..2790307hg19UCSC Ensembl
Innerchr9:2681186..2780307hg18UCSC Ensembl
Innerchr9:2681186..2780307hg17UCSC Ensembl
Cytoband9p24.2
Allele length
AssemblyAllele length
hg3899122
hg1999122
hg1899122
hg1799122
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516425
Supporting Variants
Samples
Known GenesKCNV2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv668433
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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