A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13764250



Internal ID407054
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:43464267..43473168hg38UCSC Ensembl
Innerchr10:43464327..43473109hg38UCSC Ensembl
Outerchr10:43464208..43473228hg38UCSC Ensembl
chr10:43959715..43968616hg19UCSC Ensembl
Innerchr10:43959775..43968557hg19UCSC Ensembl
Outerchr10:43959656..43968676hg19UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg388902
hg198902
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3623045
Supporting Variants
SamplesHG00121
Known GenesZNF487
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13764250
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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