A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1156301



Internal ID22084777
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:2044015..2063565hg38UCSC Ensembl
Outerchr5:2038028..2069417hg38UCSC Ensembl
Innerchr5:2044129..2063679hg19UCSC Ensembl
Outerchr5:2038142..2069531hg19UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg3831390
hg1931390
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4020618
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1156301
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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