A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv613792



Internal ID16401201
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:23171517..23186455hg38UCSC Ensembl
Innerchr9:23171516..23186453hg19UCSC Ensembl
Innerchr9:23161516..23176453hg18UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg3814939
hg1914938
hg1814938
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12590n54
Supporting Variantsnssv1156906
Samples1782681169_A
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv613792
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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