A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv569491



Internal ID16356900
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:53968723..54105296hg38UCSC Ensembl
Innerchr15:54260920..54397493hg19UCSC Ensembl
Innerchr15:52048212..52184785hg18UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg38136574
hg19136574
hg18136574
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv843274
Samples
Known GenesUNC13C
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv569491
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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