A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv614114



Internal ID16401523
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:31110059..32128830hg38UCSC Ensembl
Innerchr9:31110057..32128828hg19UCSC Ensembl
Innerchr9:31100057..32118828hg18UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg381018772
hg191018772
hg181018772
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1132521
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv614114
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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