A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1156609



Internal ID22087010
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 Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4022721
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1156609
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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