A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1156323



Internal ID22084799
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:24778267..24781719hg38UCSC Ensembl
Outerchr5:24777997..24786817hg38UCSC Ensembl
Innerchr5:24778376..24781828hg19UCSC Ensembl
Outerchr5:24778106..24786926hg19UCSC Ensembl
Cytoband5p14.1
Allele length
AssemblyAllele length
hg388821
hg198821
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4020743
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1156323
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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