A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv568056



Internal ID16355465
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:22090440..22106108hg38UCSC Ensembl
Innerchr15:22378391..22394059hg19UCSC Ensembl
Innerchr15:19879755..19895423hg18UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg3815669
hg1915669
hg1815669
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv838134
Samples
Known GenesOR4N4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv568056
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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