A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv839283



Internal ID15786553
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:27158056..27164655hg38UCSC Ensembl
Innerchr15:27403203..27409802hg19UCSC Ensembl
Innerchr15:24985949..24992548hg18UCSC Ensembl
Cytoband15q12
Allele length
AssemblyAllele length
hg386600
hg196600
hg186600
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv568657
Supporting Variants
Samples
Known GenesGABRG3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv839283
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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