A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3623039



Internal ID7009896
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:43211997..43212499hg38UCSC Ensembl
Innerchr10:43211997..43212499hg38UCSC Ensembl
Outerchr10:43211548..43212719hg38UCSC Ensembl
chr10:43707445..43707947hg19UCSC Ensembl
Innerchr10:43707445..43707947hg19UCSC Ensembl
Outerchr10:43706996..43708167hg19UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg38503
hg19503
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13764237
SamplesNA18523
Known GenesRASGEF1A
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3623039
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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