A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3595490



Internal ID6982808
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:20880317..20885938hg38UCSC Ensembl
chr3:20921809..20927430hg19UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg385622
hg195622
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv10946136, essv10946138, essv10946135, essv10946137, essv10946134
SamplesHG00881, HG02385, NA18571, HG02402, HG01817
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3595490
Frequency
Sample Size2504
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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