A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv705895



Internal ID15442547
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:135267530..135268491hg38UCSC Ensembl
Innerchr9:138159376..138160337hg19UCSC Ensembl
Innerchr9:137299197..137300158hg18UCSC Ensembl
Innerchr9:135385321..135386282hg17UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg38962
hg19962
hg18962
hg17962
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517428
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv705895
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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