A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3596905



Internal ID6984219
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:87882409..87901230hg38UCSC Ensembl
Innerchr3:87882444..87901195hg38UCSC Ensembl
Outerchr3:87882374..87901265hg38UCSC Ensembl
chr3:87931559..87950380hg19UCSC Ensembl
Innerchr3:87931594..87950345hg19UCSC Ensembl
Outerchr3:87931524..87950415hg19UCSC Ensembl
Cytoband3p11.1
Allele length
AssemblyAllele length
hg3818822
hg1918822
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11066205, essv11066203, essv11066204
SamplesNA21115, HG03624, HG03039
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3596905
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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