A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1156353



Internal ID22084829
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:79241899..79261223hg38UCSC Ensembl
Outerchr5:79229650..79266264hg38UCSC Ensembl
Innerchr5:78537722..78557046hg19UCSC Ensembl
Outerchr5:78525473..78562087hg19UCSC Ensembl
Cytoband5q14.1
Allele length
AssemblyAllele length
hg3836615
hg1936615
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4018790
Samples
Known GenesJMY
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1156353
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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