A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv568756



Internal ID16009479
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:30644082..30675803hg38UCSC Ensembl
Innerchr15:30936285..30968006hg19UCSC Ensembl
Innerchr15:28723577..28755298hg18UCSC Ensembl
Cytoband15q13.2
Allele length
AssemblyAllele length
hg3831722
hg1931722
hg1831722
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4426n54
Supporting Variantsnssv839486
Samples
Known GenesLOC100288637
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv568756
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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