A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3595787



Internal ID6983105
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:32916316..32922819hg38UCSC Ensembl
Innerchr3:32916816..32922319hg38UCSC Ensembl
Outerchr3:32915316..32923819hg38UCSC Ensembl
chr3:32957808..32964311hg19UCSC Ensembl
Innerchr3:32958308..32963811hg19UCSC Ensembl
Outerchr3:32956808..32965311hg19UCSC Ensembl
Cytoband3p22.3
Allele length
AssemblyAllele length
hg386504
hg196504
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv10977925, essv10977923, essv10977922, essv10977926, essv10977921, essv10977927, essv10977924
SamplesHG00187, HG00281, HG02224, HG02187, NA20587, NA19403, HG00476
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3595787
Frequency
Sample Size2504
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


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