A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3596903



Internal ID6984217
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:87854332..87902304hg38UCSC Ensembl
Innerchr3:87854332..87902304hg38UCSC Ensembl
Outerchr3:87853832..87902804hg38UCSC Ensembl
chr3:87903482..87951454hg19UCSC Ensembl
Innerchr3:87903482..87951454hg19UCSC Ensembl
Outerchr3:87902982..87951954hg19UCSC Ensembl
Cytoband3p11.1
Allele length
AssemblyAllele length
hg3847973
hg1947973
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11066175, essv11066176
SamplesNA21115, HG03624
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3596903
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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