A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv561258



Internal ID16348667
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:21412181..21484214hg38UCSC Ensembl
Innerchr13:21986320..22058353hg19UCSC Ensembl
Innerchr13:20884320..20956353hg18UCSC Ensembl
Cytoband13q12.11
Allele length
AssemblyAllele length
hg3872034
hg1972034
hg1872034
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv806194
Samples
Known GenesZDHHC20
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv561258
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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