A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4008159



Internal ID22069790
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:64726321..64740963hg38UCSC Ensembl
Outerchr13:64708530..64745216hg38UCSC Ensembl
Innerchr13:65300453..65315095hg19UCSC Ensembl
Outerchr13:65282662..65319348hg19UCSC Ensembl
Cytoband13q21.31
Allele length
AssemblyAllele length
hg3836687
hg1936687
Variant TypeCNV duplication
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1154922
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4008159
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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