A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3623854



Internal ID7010710
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:75737225..75742724hg38UCSC Ensembl
Innerchr10:75737225..75742724hg38UCSC Ensembl
Outerchr10:75736725..75743224hg38UCSC Ensembl
chr10:77496983..77502482hg19UCSC Ensembl
Innerchr10:77496983..77502482hg19UCSC Ensembl
Outerchr10:77496483..77502982hg19UCSC Ensembl
Cytoband10q22.2
Allele length
AssemblyAllele length
hg385500
hg195500
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13864450
SamplesNA19149
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3623854
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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