A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv613848



Internal ID16401257
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:24152520..24258865hg38UCSC Ensembl
Innerchr9:24152518..24258863hg19UCSC Ensembl
Innerchr9:24142518..24248863hg18UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg38106346
hg19106346
hg18106346
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1131863
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv613848
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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