A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv568919



Internal ID16356328
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:33346134..33444482hg38UCSC Ensembl
Innerchr15:33638335..33736683hg19UCSC Ensembl
Innerchr15:31425627..31523975hg18UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg3898349
hg1998349
hg1898349
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv839797
Samples
Known GenesRYR3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv568919
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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