A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv613920



Internal ID16054643
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:25919853..25971499hg38UCSC Ensembl
Innerchr9:25919851..25971497hg19UCSC Ensembl
Innerchr9:25909851..25961497hg18UCSC Ensembl
Cytoband9p21.2
Allele length
AssemblyAllele length
hg3851647
hg1951647
hg1851647
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1156741
Samples1780862001_A
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv613920
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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