A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv614960



Internal ID16402369
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:100998502..100999836hg38UCSC Ensembl
Innerchr9:103760784..103762118hg19UCSC Ensembl
Innerchr9:102800605..102801939hg18UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg381335
hg191335
hg181335
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12810n54
Supporting Variantsnssv1140220
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv614960
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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