A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4008264



Internal ID22069895
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:81114226..81135511hg38UCSC Ensembl
Outerchr13:81111157..81137787hg38UCSC Ensembl
Innerchr13:81688361..81709646hg19UCSC Ensembl
Outerchr13:81685292..81711922hg19UCSC Ensembl
Cytoband13q31.1
Allele length
AssemblyAllele length
hg3826631
hg1926631
Variant TypeCNV duplication
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1154944
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4008264
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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