A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3595806



Internal ID6983124
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:34191401..34205031hg38UCSC Ensembl
Innerchr3:34191401..34205031hg38UCSC Ensembl
Outerchr3:34190901..34205531hg38UCSC Ensembl
chr3:34232893..34246523hg19UCSC Ensembl
Innerchr3:34232893..34246523hg19UCSC Ensembl
Outerchr3:34232393..34247023hg19UCSC Ensembl
Cytoband3p22.3
Allele length
AssemblyAllele length
hg3813631
hg1913631
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv10979499
SamplesHG02184
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3595806
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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