A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv569194



Internal ID16356603
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:36375572..36416091hg38UCSC Ensembl
Innerchr15:36667773..36708292hg19UCSC Ensembl
Innerchr15:34455065..34495584hg18UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg3840520
hg1940520
hg1840520
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4494n54
Supporting Variantsnssv840695
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv569194
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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