A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3623063



Internal ID7009920
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:44390011..44399862hg38UCSC Ensembl
Innerchr10:44390020..44399854hg38UCSC Ensembl
Outerchr10:44390003..44399871hg38UCSC Ensembl
chr10:44885459..44895310hg19UCSC Ensembl
Innerchr10:44885468..44895302hg19UCSC Ensembl
Outerchr10:44885451..44895319hg19UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg389852
hg199852
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13765003, essv13765004
SamplesHG03690, HG00306
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3623063
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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