A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv703870



Internal ID15440522
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:4331717..4447405hg38UCSC Ensembl
Innerchr9:4331717..4447405hg19UCSC Ensembl
Innerchr9:4321717..4437405hg18UCSC Ensembl
Innerchr9:4321717..4437405hg17UCSC Ensembl
Cytoband9p24.2
Allele length
AssemblyAllele length
hg38115689
hg19115689
hg18115689
hg17115689
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv527431
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv703870
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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