A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1156763



Internal ID22087164
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 Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4019733
Samples
Known GenesDPP6
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1156763
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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