A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv569541



Internal ID16356950
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:55638344..55690059hg38UCSC Ensembl
Innerchr15:55930542..55982257hg19UCSC Ensembl
Innerchr15:53717834..53769549hg18UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg3851716
hg1951716
hg1851716
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1148878
SamplesHGDP01164
Known GenesPRTG
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv569541
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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