A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3622654



Internal ID7009512
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:24826554..24832234hg38UCSC Ensembl
Innerchr10:24827054..24831734hg38UCSC Ensembl
Outerchr10:24825554..24833234hg38UCSC Ensembl
chr10:25115483..25121163hg19UCSC Ensembl
Innerchr10:25115983..25120663hg19UCSC Ensembl
Outerchr10:25114483..25122163hg19UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg385681
hg195681
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13721432, essv13721434, essv13721433, essv13721431
SamplesHG02050, NA18542, NA18740, NA18612
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3622654
Frequency
Sample Size2504
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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