A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3622562



Internal ID7009421
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:20573444..20604654hg38UCSC Ensembl
Innerchr10:20573444..20604654hg38UCSC Ensembl
Outerchr10:20572944..20605154hg38UCSC Ensembl
chr10:20862373..20893583hg19UCSC Ensembl
Innerchr10:20862373..20893583hg19UCSC Ensembl
Outerchr10:20861873..20894083hg19UCSC Ensembl
Cytoband10p12.31
Allele length
AssemblyAllele length
hg3831211
hg1931211
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13714413
SamplesHG01353
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3622562
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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