A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4006678



Internal ID22068309
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:105049259..105057802hg38UCSC Ensembl
Outerchr9:105048619..105060185hg38UCSC Ensembl
Innerchr9:107811540..107820083hg19UCSC Ensembl
Outerchr9:107810900..107822466hg19UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg3811567
hg1911567
Variant TypeCNV duplication
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1154523
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4006678
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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