A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv615182



Internal ID16402591
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:111123414..111226880hg38UCSC Ensembl
Innerchr9:113885694..113989160hg19UCSC Ensembl
Innerchr9:112925515..113028981hg18UCSC Ensembl
Cytoband9q31.3
Allele length
AssemblyAllele length
hg38103467
hg19103467
hg18103467
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1176118
SamplesNINDS_26
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv615182
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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