A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv570562



Internal ID16357971
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:94572764..94972628hg38UCSC Ensembl
Innerchr15:95115993..95515857hg19UCSC Ensembl
Innerchr15:92916997..93316861hg18UCSC Ensembl
Cytoband15q26.2
Allele length
AssemblyAllele length
hg38399865
hg19399865
hg18399865
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv849045
Samples
Known GenesLOC440311
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv570562
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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