A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv568659



Internal ID16356068
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:27160738..27164848hg38UCSC Ensembl
Innerchr15:27405885..27409995hg19UCSC Ensembl
Innerchr15:24988631..24992741hg18UCSC Ensembl
Cytoband15q12
Allele length
AssemblyAllele length
hg384111
hg194111
hg184111
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4409n54
Supporting Variantsnssv839286
Samples
Known GenesGABRG3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv568659
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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