A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv569197



Internal ID16356606
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:36670330..36734364hg38UCSC Ensembl
Innerchr15:36962531..37026565hg19UCSC Ensembl
Innerchr15:34749823..34813857hg18UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg3864035
hg1964035
hg1864035
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv840700
Samples
Known GenesC15orf41
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv569197
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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