A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3623865



Internal ID6664032
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:76353972..76356616hg38UCSC Ensembl
Innerchr10:76353972..76356616hg38UCSC Ensembl
Outerchr10:76353748..76356815hg38UCSC Ensembl
chr10:78113730..78116374hg19UCSC Ensembl
Innerchr10:78113730..78116374hg19UCSC Ensembl
Outerchr10:78113506..78116573hg19UCSC Ensembl
Cytoband10q22.3
Allele length
AssemblyAllele length
hg382645
hg192645
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13864511, essv13864512
SamplesHG00698, HG00559
Known GenesC10orf11
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3623865
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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