A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4018938



Internal ID22080569
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:91945393..91994186hg38UCSC Ensembl
Outerchr5:91939631..91995892hg38UCSC Ensembl
Innerchr5:91241210..91290003hg19UCSC Ensembl
Outerchr5:91235448..91291709hg19UCSC Ensembl
Cytoband5q14.3
Allele length
AssemblyAllele length
hg3856262
hg1956262
Variant TypeCNV duplication
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1156362
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4018938
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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