A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4016094



Internal ID22077725
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:163877778..164177912hg38UCSC Ensembl
Outerchr3:163874417..164188095hg38UCSC Ensembl
Innerchr3:163595566..163895700hg19UCSC Ensembl
Outerchr3:163592205..163905883hg19UCSC Ensembl
Cytoband3q26.1
Allele length
AssemblyAllele length
hg38313679
hg19313679
Variant TypeCNV duplication
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1156041
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4016094
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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