A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv569241



Internal ID16009964
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:42908911..43230724hg38UCSC Ensembl
Innerchr15:43201109..43522922hg19UCSC Ensembl
Innerchr15:40988401..41310214hg18UCSC Ensembl
Cytoband15q15.2
Allele length
AssemblyAllele length
hg38321814
hg19321814
hg18321814
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv842230
Samples
Known GenesCCNDBP1, EPB42, TMEM62, TTBK2, UBR1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv569241
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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