A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4021102



Internal ID22082733
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:39514211..39526962hg38UCSC Ensembl
Outerchr7:39510390..39530900hg38UCSC Ensembl
Innerchr7:39553810..39566561hg19UCSC Ensembl
Outerchr7:39549989..39570499hg19UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg3820511
hg1920511
Variant TypeCNV deletion
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1156656
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4021102
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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