A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3595796



Internal ID6983114
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:33778849..33787256hg38UCSC Ensembl
Innerchr3:33778874..33787231hg38UCSC Ensembl
Outerchr3:33778824..33787281hg38UCSC Ensembl
chr3:33820341..33828748hg19UCSC Ensembl
Innerchr3:33820366..33828723hg19UCSC Ensembl
Outerchr3:33820316..33828773hg19UCSC Ensembl
Cytoband3p22.3
Allele length
AssemblyAllele length
hg388408
hg198408
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv10979333, essv10979332, essv10979335, essv10979331, essv10979336, essv10979334, essv10979337
SamplesNA12273, HG00367, HG01779, HG01459, HG01187, NA19670, HG01623
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3595796
Frequency
Sample Size2504
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


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