A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv569683



Internal ID16357092
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:62414365..62428164hg38UCSC Ensembl
Innerchr15:62706564..62720363hg19UCSC Ensembl
Innerchr15:60493856..60507655hg18UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg3813800
hg1913800
hg1813800
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4567n54
Supporting Variantsnssv843926
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv569683
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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