A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3622206



Internal ID7009065
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:4679251..4681948hg38UCSC Ensembl
Innerchr10:4679292..4681908hg38UCSC Ensembl
Outerchr10:4679211..4681989hg38UCSC Ensembl
chr10:4721443..4724140hg19UCSC Ensembl
Innerchr10:4721484..4724100hg19UCSC Ensembl
Outerchr10:4721403..4724181hg19UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg382698
hg192698
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13685243, essv13685241, essv13685240, essv13685238, essv13685244, essv13685239, essv13685245, essv13685242
SamplesHG00142, NA20531, HG01682, NA10847, HG01501, NA19072, HG01623, NA20807
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3622206
Frequency
Sample Size2504
Observed Gain0
Observed Loss8
Observed Complex0
Frequencyn/a


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