A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1156881



Internal ID22087282
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:20403160..20414361hg38UCSC Ensembl
Outerchr8:20401438..20417701hg38UCSC Ensembl
Innerchr8:20260671..20271872hg19UCSC Ensembl
Outerchr8:20258949..20275212hg19UCSC Ensembl
Cytoband8p21.3
Allele length
AssemblyAllele length
hg3816264
hg1916264
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4020974
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1156881
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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