A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv839790



Internal ID15787060
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:32609219..32622120hg38UCSC Ensembl
Innerchr15:32901420..32914321hg19UCSC Ensembl
Innerchr15:30688712..30701613hg18UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg3812902
hg1912902
hg1812902
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv568911
Supporting Variants
Samples
Known GenesARHGAP11A
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv839790
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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