A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4010182



Internal ID22071813
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:36022799..36031802hg38UCSC Ensembl
Outerchr17:36019230..36032689hg38UCSC Ensembl
Innerchr17:34349836..34358839hg19UCSC Ensembl
Outerchr17:34346267..34359725hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg3813460
hg1913459
Variant TypeCNV duplication
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1155398
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4010182
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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