A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv568678



Internal ID16009401
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:29090260..29120363hg38UCSC Ensembl
Innerchr15:29382463..29412566hg19UCSC Ensembl
Innerchr15:27169755..27199858hg18UCSC Ensembl
Cytoband15q13.1
Allele length
AssemblyAllele length
hg3830104
hg1930104
hg1830104
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv839309
Samples
Known GenesAPBA2, FAM189A1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv568678
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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