A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4018993



Internal ID22080624
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:115370746..115385388hg38UCSC Ensembl
Outerchr5:115369510..115387269hg38UCSC Ensembl
Innerchr5:114706443..114721085hg19UCSC Ensembl
Outerchr5:114705207..114722966hg19UCSC Ensembl
Cytoband5q22.3
Allele length
AssemblyAllele length
hg3817760
hg1917760
Variant TypeCNV deletion
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1156378
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4018993
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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