A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3605718



Internal ID6992656
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:87038548..87057985hg38UCSC Ensembl
Innerchr5:87039048..87057485hg38UCSC Ensembl
Outerchr5:87037548..87058985hg38UCSC Ensembl
chr5:86334365..86353802hg19UCSC Ensembl
Innerchr5:86334865..86353302hg19UCSC Ensembl
Outerchr5:86333365..86354802hg19UCSC Ensembl
Cytoband5q14.3
Allele length
AssemblyAllele length
hg3819438
hg1919438
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11966977
SamplesHG03714
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3605718
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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