A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3623957



Internal ID7010813
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:80809339..80815141hg38UCSC Ensembl
Innerchr10:80809401..80815079hg38UCSC Ensembl
Outerchr10:80809277..80815203hg38UCSC Ensembl
chr10:82569095..82574897hg19UCSC Ensembl
Innerchr10:82569157..82574835hg19UCSC Ensembl
Outerchr10:82569033..82574959hg19UCSC Ensembl
Cytoband10q23.1
Allele length
AssemblyAllele length
hg385803
hg195803
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13870845
SamplesHG00560
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3623957
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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