A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3623858



Internal ID6664025
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:76076016..76078599hg38UCSC Ensembl
Innerchr10:76076066..76078549hg38UCSC Ensembl
Outerchr10:76075952..76078663hg38UCSC Ensembl
chr10:77835774..77838357hg19UCSC Ensembl
Innerchr10:77835824..77838307hg19UCSC Ensembl
Outerchr10:77835710..77838421hg19UCSC Ensembl
Cytoband10q22.3
Allele length
AssemblyAllele length
hg382584
hg192584
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13864456, essv13864457, essv13864455
SamplesHG03066, HG03428, HG02819
Known GenesC10orf11
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3623858
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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