A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3622744



Internal ID7009602
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:28360140..28368206hg38UCSC Ensembl
Innerchr10:28360140..28368206hg38UCSC Ensembl
Outerchr10:28359640..28368706hg38UCSC Ensembl
chr10:28649069..28657135hg19UCSC Ensembl
Innerchr10:28649069..28657135hg19UCSC Ensembl
Outerchr10:28648569..28657635hg19UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg388067
hg198067
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13737854
SamplesHG01992
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3622744
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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