A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4022162



Internal ID22083793
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:86604868..86615738hg38UCSC Ensembl
Outerchr7:86600286..86622960hg38UCSC Ensembl
Innerchr7:86234184..86245054hg19UCSC Ensembl
Outerchr7:86229602..86252276hg19UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg3822675
hg1922675
Variant TypeCNV deletion
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1156694
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4022162
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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