A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3622234



Internal ID7009093
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:5804504..5809863hg38UCSC Ensembl
Innerchr10:5804504..5809863hg38UCSC Ensembl
Outerchr10:5804369..5809996hg38UCSC Ensembl
chr10:5846467..5851826hg19UCSC Ensembl
Innerchr10:5846467..5851826hg19UCSC Ensembl
Outerchr10:5846332..5851959hg19UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg385360
hg195360
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13685665
SamplesHG02337
Known GenesGDI2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3622234
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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