A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3591123



Internal ID6631407
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:66610068..66619222hg38UCSC Ensembl
Innerchr2:66610104..66619186hg38UCSC Ensembl
Outerchr2:66610032..66619258hg38UCSC Ensembl
chr2:66837200..66846354hg19UCSC Ensembl
Innerchr2:66837236..66846318hg19UCSC Ensembl
Outerchr2:66837164..66846390hg19UCSC Ensembl
Cytoband2p14
Allele length
AssemblyAllele length
hg389155
hg199155
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv10532378
SamplesHG01708
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3591123
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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