A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv569652



Internal ID16357061
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:62047927..62102125hg38UCSC Ensembl
Innerchr15:62340126..62394324hg19UCSC Ensembl
Innerchr15:60127418..60181616hg18UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg3854199
hg1954199
hg1854199
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1149229
SamplesHGDP00966
Known GenesC2CD4A, VPS13C
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv569652
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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