A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3594163



Internal ID6981483
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:211027369..211036891hg38UCSC Ensembl
Innerchr2:211027411..211036849hg38UCSC Ensembl
Outerchr2:211027327..211036933hg38UCSC Ensembl
chr2:211892093..211901615hg19UCSC Ensembl
Innerchr2:211892135..211901573hg19UCSC Ensembl
Outerchr2:211892051..211901657hg19UCSC Ensembl
Cytoband2q34
Allele length
AssemblyAllele length
hg389523
hg199523
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv10835516
SamplesNA19474
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3594163
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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