A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv695847



Internal ID15432499
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:8009428..8012608hg38UCSC Ensembl
Innerchr9:8009428..8012608hg19UCSC Ensembl
Innerchr9:7999428..8002608hg18UCSC Ensembl
Innerchr9:7999428..8002608hg17UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg383181
hg193181
hg183181
hg173181
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv519428
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv695847
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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