A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3622197



Internal ID7009056
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:4473783..4488258hg38UCSC Ensembl
Innerchr10:4473800..4488241hg38UCSC Ensembl
Outerchr10:4473766..4488275hg38UCSC Ensembl
chr10:4515975..4530450hg19UCSC Ensembl
Innerchr10:4515992..4530433hg19UCSC Ensembl
Outerchr10:4515958..4530467hg19UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg3814476
hg1914476
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13682923, essv13682922
SamplesHG03812, HG03595
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3622197
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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