A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4020805



Internal ID22082436
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:41231396..41241291hg38UCSC Ensembl
Outerchr5:41226663..41244575hg38UCSC Ensembl
Innerchr5:41231498..41241393hg19UCSC Ensembl
Outerchr5:41226765..41244677hg19UCSC Ensembl
Cytoband5p13.1
Allele length
AssemblyAllele length
hg3817913
hg1917913
Variant TypeCNV deletion
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1156332
Supporting Variants
Samples
Known GenesC6
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4020805
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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