A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1156379



Internal ID22086780
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:115370746..115387347hg38UCSC Ensembl
Outerchr5:115369510..115388503hg38UCSC Ensembl
Innerchr5:114706443..114723044hg19UCSC Ensembl
Outerchr5:114705207..114724200hg19UCSC Ensembl
Cytoband5q22.3
Allele length
AssemblyAllele length
hg3818994
hg1918994
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv233n97
Supporting Variantsnssv4018995
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1156379
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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