A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3623696



Internal ID7010552
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:67927566..67931844hg38UCSC Ensembl
Innerchr10:67927716..67931694hg38UCSC Ensembl
Outerchr10:67927416..67931994hg38UCSC Ensembl
chr10:69687323..69691601hg19UCSC Ensembl
Innerchr10:69687473..69691451hg19UCSC Ensembl
Outerchr10:69687173..69691751hg19UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg384279
hg194279
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13848634
SamplesHG00607
Known GenesHERC4
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3623696
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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