A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv527389



Internal ID15454682
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:13380508..13388039hg38UCSC Ensembl
Innerchr9:13380507..13388038hg19UCSC Ensembl
Innerchr9:13370507..13378038hg18UCSC Ensembl
Innerchr9:13370507..13378038hg17UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg387532
hg197532
hg187532
hg177532
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv703824
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv527389
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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