A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13933221



Internal ID4503276
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:109824968..109828390hg38UCSC Ensembl
Innerchr10:109825008..109828351hg38UCSC Ensembl
Outerchr10:109824929..109828430hg38UCSC Ensembl
chr10:111584726..111588148hg19UCSC Ensembl
Innerchr10:111584766..111588109hg19UCSC Ensembl
Outerchr10:111584687..111588188hg19UCSC Ensembl
Cytoband10q25.1
Allele length
AssemblyAllele length
hg383423
hg193423
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3624529
Supporting Variants
SamplesHG04002
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13933221
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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