A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4004706



Internal ID22066337
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:32167619..32211397hg38UCSC Ensembl
Outerchr10:32165341..32218336hg38UCSC Ensembl
Innerchr10:32456547..32500325hg19UCSC Ensembl
Outerchr10:32454269..32507264hg19UCSC Ensembl
Cytoband10p11.22
Allele length
AssemblyAllele length
hg3852996
hg1952996
Variant TypeCNV duplication
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1154571
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4004706
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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