A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1156460



Internal ID22086861
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:19816626..19819677hg38UCSC Ensembl
Outerchr6:19810194..19821095hg38UCSC Ensembl
Innerchr6:19816857..19819908hg19UCSC Ensembl
Outerchr6:19810425..19821326hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg3810902
hg1910902
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4018315
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1156460
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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