A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4018099



Internal ID22079730
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:178682974..178686162hg38UCSC Ensembl
Outerchr5:178680821..178691854hg38UCSC Ensembl
Innerchr5:178109975..178113163hg19UCSC Ensembl
Outerchr5:178107822..178118855hg19UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg3811034
hg1911034
Variant TypeCNV deletion
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1156416
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4018099
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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