A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3622127



Internal ID7008986
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:2355072..2361831hg38UCSC Ensembl
Innerchr10:2355086..2361817hg38UCSC Ensembl
Outerchr10:2355058..2361845hg38UCSC Ensembl
chr10:2397266..2404025hg19UCSC Ensembl
Innerchr10:2397280..2404011hg19UCSC Ensembl
Outerchr10:2397252..2404039hg19UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg386760
hg196760
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13669398
SamplesHG03792
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3622127
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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