A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv844371



Internal ID15791641
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:69215121..69232379hg38UCSC Ensembl
Innerchr15:69507460..69524718hg19UCSC Ensembl
Innerchr15:67294514..67311772hg18UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg3817259
hg1917259
hg1817259
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv569812
Supporting Variants
Samples
Known GenesGLCE
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv844371
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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