A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4004712



Internal ID22066343
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:43515126..43518045hg38UCSC Ensembl
Outerchr10:43510404..43519905hg38UCSC Ensembl
Innerchr10:44010574..44013493hg19UCSC Ensembl
Outerchr10:44005852..44015353hg19UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg389502
hg199502
Variant TypeCNV duplication
Copy Number4
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1154578
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4004712
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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