A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv569690



Internal ID16357099
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:63189396..63190494hg38UCSC Ensembl
Innerchr15:63481595..63482693hg19UCSC Ensembl
Innerchr15:61268648..61269746hg18UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg381099
hg191099
hg181099
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv843952
Samples
Known GenesRAB8B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv569690
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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