A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3624529



Internal ID7011382
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 State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13933221
SamplesHG04002
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3624529
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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