A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4022227



Internal ID22083858
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:120996879..121016574hg38UCSC Ensembl
Outerchr7:120996742..121020676hg38UCSC Ensembl
Innerchr7:120636933..120656628hg19UCSC Ensembl
Outerchr7:120636796..120660730hg19UCSC Ensembl
Cytoband7q31.31
Allele length
AssemblyAllele length
hg3823935
hg1923935
Variant TypeCNV deletion
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1156721
Supporting Variants
Samples
Known GenesCPED1
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4022227
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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