A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv808001



Internal ID16101957
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:38080909..38126909hg38UCSC Ensembl
Innerchr13:38655046..38701046hg19UCSC Ensembl
Innerchr13:37553046..37599046hg18UCSC Ensembl
Cytoband13q13.3
Allele length
AssemblyAllele length
hg3846001
hg1946001
hg1846001
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv561511
Supporting Variants
Samples
Known GenesLINC00571
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv808001
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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