A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv615261



Internal ID16402670
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:116980695..117151329hg38UCSC Ensembl
Innerchr9:119742974..119913608hg19UCSC Ensembl
Innerchr9:118782795..118953429hg18UCSC Ensembl
Cytoband9q33.1
Allele length
AssemblyAllele length
hg38170635
hg19170635
hg18170635
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1141288
Samples
Known GenesASTN2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv615261
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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