A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3591064



Internal ID6978392
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:63764231..63767796hg38UCSC Ensembl
Innerchr2:63764261..63767767hg38UCSC Ensembl
Outerchr2:63764202..63767826hg38UCSC Ensembl
chr2:63991365..63994930hg19UCSC Ensembl
Innerchr2:63991395..63994901hg19UCSC Ensembl
Outerchr2:63991336..63994960hg19UCSC Ensembl
Cytoband2p15
Allele length
AssemblyAllele length
hg383566
hg193566
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv10524759
SamplesHG01801
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3591064
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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