A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3591778



Internal ID6979106
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:101961771..101963351hg38UCSC Ensembl
Innerchr2:101961789..101963334hg38UCSC Ensembl
Outerchr2:101961754..101963369hg38UCSC Ensembl
chr2:102578233..102579813hg19UCSC Ensembl
Innerchr2:102578251..102579796hg19UCSC Ensembl
Outerchr2:102578216..102579831hg19UCSC Ensembl
Cytoband2q11.2
Allele length
AssemblyAllele length
hg381581
hg191581
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv10597851
SamplesHG02643
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3591778
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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