A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13848634



Internal ID976769
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3623696
Supporting Variants
SamplesHG00607
Known GenesHERC4
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13848634
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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