A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv569248



Internal ID16356657
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:43601620..43688207hg38UCSC Ensembl
Innerchr15:43893818..43980405hg19UCSC Ensembl
Innerchr15:41681110..41767697hg18UCSC Ensembl
Cytoband15q15.3
Allele length
AssemblyAllele length
hg3886588
hg1986588
hg1886588
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4501n54
Supporting Variantsnssv842241
Samples
Known GenesCATSPER2, RNU6-28P, STRC
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv569248
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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