A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2657079



Internal ID9576498
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:151410503..151413348hg38UCSC Ensembl
Outerchr5:151410466..151413398hg38UCSC Ensembl
Innerchr5:150790064..150792909hg19UCSC Ensembl
Outerchr5:150790027..150792959hg19UCSC Ensembl
Cytoband5q33.1
Allele length
AssemblyAllele length
hg382933
hg192933
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1049e199
Supporting Variantsessv6461158, essv6079718, essv5454428, essv5968190
SamplesHG00524, HG01051, NA12341, NA19716
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2657079
Frequency
Sample Size1151
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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