A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv613449



Internal ID16400858
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:11745912..12220126hg38UCSC Ensembl
Innerchr9:11745912..12220126hg19UCSC Ensembl
Innerchr9:11735912..12210126hg18UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg38474215
hg19474215
hg18474215
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1128572
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv613449
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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