A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13854998



Internal ID5726886
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:69280069..69294203hg38UCSC Ensembl
Innerchr10:69280569..69293703hg38UCSC Ensembl
Outerchr10:69279069..69295203hg38UCSC Ensembl
chr10:71039825..71053959hg19UCSC Ensembl
Innerchr10:71040325..71053459hg19UCSC Ensembl
Outerchr10:71038825..71054959hg19UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg3814135
hg1914135
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3623739
Supporting Variants
SamplesNA19102
Known GenesHK1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13854998
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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