A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3623257



Internal ID7010114
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:52741372..52742980hg38UCSC Ensembl
Innerchr10:52741383..52742970hg38UCSC Ensembl
Outerchr10:52741362..52742991hg38UCSC Ensembl
chr10:54501132..54502740hg19UCSC Ensembl
Innerchr10:54501143..54502730hg19UCSC Ensembl
Outerchr10:54501122..54502751hg19UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg381609
hg191609
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13810903
SamplesHG01699
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3623257
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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