A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv569231



Internal ID16009954
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:41118507..41254433hg38UCSC Ensembl
Innerchr15:41410705..41546631hg19UCSC Ensembl
Innerchr15:39197997..39333923hg18UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg38135927
hg19135927
hg18135927
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv842222
Samples
Known GenesCHP1, EXD1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv569231
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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