A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3596897



Internal ID6637167
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:87803460..87899387hg38UCSC Ensembl
chr3:87852610..87948537hg19UCSC Ensembl
Cytoband3p11.1
Allele length
AssemblyAllele length
hg3895928
hg1995928
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11066115
SamplesHG03624
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3596897
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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