A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv694552



Internal ID15431204
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:2699004..2699606hg38UCSC Ensembl
Innerchr9:2699004..2699606hg19UCSC Ensembl
Innerchr9:2689004..2689606hg18UCSC Ensembl
Innerchr9:2689004..2689606hg17UCSC Ensembl
Cytoband9p24.2
Allele length
AssemblyAllele length
hg38603
hg19603
hg18603
hg17603
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516425
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv694552
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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