A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3622186



Internal ID7009045
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:4108478..4117931hg38UCSC Ensembl
Innerchr10:4108528..4117881hg38UCSC Ensembl
Outerchr10:4108428..4117981hg38UCSC Ensembl
chr10:4150670..4160123hg19UCSC Ensembl
Innerchr10:4150720..4160073hg19UCSC Ensembl
Outerchr10:4150620..4160173hg19UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg389454
hg199454
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13680556
SamplesHG03280
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3622186
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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