A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13867031



Internal ID3868847
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:79122094..79142496hg38UCSC Ensembl
Innerchr10:79122104..79142486hg38UCSC Ensembl
Outerchr10:79122084..79142506hg38UCSC Ensembl
chr10:80881851..80902253hg19UCSC Ensembl
Innerchr10:80881861..80902243hg19UCSC Ensembl
Outerchr10:80881841..80902263hg19UCSC Ensembl
Cytoband10q22.3
Allele length
AssemblyAllele length
hg3820403
hg1920403
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3623907
Supporting Variants
SamplesHG01790
Known GenesZMIZ1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13867031
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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