A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4020806



Internal ID22082437
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:41587169..41595002hg38UCSC Ensembl
Outerchr5:41583900..41599347hg38UCSC Ensembl
Innerchr5:41587271..41595104hg19UCSC Ensembl
Outerchr5:41584002..41599449hg19UCSC Ensembl
Cytoband5p13.1
Allele length
AssemblyAllele length
hg3815448
hg1915448
Variant TypeCNV deletion
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1156333
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4020806
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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