A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3623054



Internal ID7009911
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:44022458..44026932hg38UCSC Ensembl
Innerchr10:44022492..44026898hg38UCSC Ensembl
Outerchr10:44022424..44026966hg38UCSC Ensembl
chr10:44517906..44522380hg19UCSC Ensembl
Innerchr10:44517940..44522346hg19UCSC Ensembl
Outerchr10:44517872..44522414hg19UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg384475
hg194475
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13764553, essv13764554
SamplesNA18977, HG03458
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3623054
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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