A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4022721



Internal ID22084352
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:163987184..164664015hg38UCSC Ensembl
Outerchr6:163986265..164668000hg38UCSC Ensembl
Innerchr6:164408216..165085048hg19UCSC Ensembl
Outerchr6:164407297..165089033hg19UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg38681736
hg19681737
Variant TypeCNV duplication
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1156609
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4022721
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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