A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv569229



Internal ID16009952
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:41068940..41191484hg38UCSC Ensembl
Innerchr15:41361138..41483682hg19UCSC Ensembl
Innerchr15:39148430..39270974hg18UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg38122545
hg19122545
hg18122545
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4499n54
Supporting Variantsnssv842220
Samples
Known GenesEXD1, INO80
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv569229
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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