A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4008270



Internal ID22069901
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:84670431..84711720hg38UCSC Ensembl
Outerchr13:84665189..84718257hg38UCSC Ensembl
Innerchr13:85244566..85285855hg19UCSC Ensembl
Outerchr13:85239324..85292392hg19UCSC Ensembl
Cytoband13q31.1
Allele length
AssemblyAllele length
hg3853069
hg1953069
Variant TypeCNV duplication
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1154951
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4008270
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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