A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3624411



Internal ID6664578
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:103309958..103311178hg38UCSC Ensembl
Innerchr10:103310008..103311128hg38UCSC Ensembl
Outerchr10:103309887..103311249hg38UCSC Ensembl
chr10:105069715..105070935hg19UCSC Ensembl
Innerchr10:105069765..105070885hg19UCSC Ensembl
Outerchr10:105069644..105071006hg19UCSC Ensembl
Cytoband10q24.33
Allele length
AssemblyAllele length
hg381221
hg191221
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13914612, essv13914610, essv13914609, essv13914607, essv13914608, essv13914606, essv13914611
SamplesNA19474, NA19428, NA19443, HG03559, NA19440, HG02325, HG03557
Known GenesPCGF6
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3624411
Frequency
Sample Size2504
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


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