A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526799



Internal ID15454092
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:24332123..24385359hg38UCSC Ensembl
Innerchr9:24332121..24385357hg19UCSC Ensembl
Innerchr9:24322121..24375357hg18UCSC Ensembl
Innerchr9:24322121..24375357hg17UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg3853237
hg1953237
hg1853237
hg1753237
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv703153
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526799
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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