A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv843961



Internal ID16137917
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:63189850..63190597hg38UCSC Ensembl
Innerchr15:63482049..63482796hg19UCSC Ensembl
Innerchr15:61269102..61269849hg18UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg38748
hg19748
hg18748
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv569695
Supporting Variants
Samples
Known GenesRAB8B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv843961
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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