A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv613635



Internal ID16401044
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:13893247..13961463hg38UCSC Ensembl
Innerchr9:13893246..13961462hg19UCSC Ensembl
Innerchr9:13883246..13951462hg18UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg3868217
hg1968217
hg1868217
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1128779
Samples
Known GenesLINC00583
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv613635
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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