A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4021964



Internal ID22083595
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:158961941..159198763hg38UCSC Ensembl
Outerchr7:158961557..159205468hg38UCSC Ensembl
Innerchr7:158754632..158991452hg19UCSC Ensembl
Outerchr7:158754248..158998157hg19UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg38243912
hg19243910
Variant TypeCNV duplication
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1156772
Supporting Variants
Samples
Known GenesLINC00689, VIPR2
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4021964
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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