A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1156610



Internal ID22087011
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:164709985..164774062hg38UCSC Ensembl
Outerchr6:164702603..164790550hg38UCSC Ensembl
Innerchr6:165131018..165195092hg19UCSC Ensembl
Outerchr6:165123636..165204063hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg3887948
hg1980428
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4022722
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1156610
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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