A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4011863



Internal ID22073494
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:54121666..54201545hg38UCSC Ensembl
Outerchr17:54117666..54207798hg38UCSC Ensembl
Innerchr17:52199027..52278906hg19UCSC Ensembl
Outerchr17:52195027..52285159hg19UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg3890133
hg1990133
Variant TypeCNV duplication
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1155484
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4011863
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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