A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4019733



Internal ID22081364
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:153971534..154151922hg38UCSC Ensembl
Outerchr7:153969863..154154451hg38UCSC Ensembl
Innerchr7:153668619..153849007hg19UCSC Ensembl
Outerchr7:153666948..153851536hg19UCSC Ensembl
Cytoband7q36.2
Allele length
AssemblyAllele length
hg38184589
hg19184589
Variant TypeCNV duplication
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1156763
Supporting Variants
Samples
Known GenesDPP6
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4019733
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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