A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13810903



Internal ID1827458
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3623257
Supporting Variants
SamplesHG01699
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13810903
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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