A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3623814



Internal ID7010670
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:73544490..73555755hg38UCSC Ensembl
Innerchr10:73544532..73555713hg38UCSC Ensembl
Outerchr10:73544448..73555797hg38UCSC Ensembl
chr10:75304248..75315513hg19UCSC Ensembl
Innerchr10:75304290..75315471hg19UCSC Ensembl
Outerchr10:75304206..75315555hg19UCSC Ensembl
Cytoband10q22.2
Allele length
AssemblyAllele length
hg3811266
hg1911266
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13861915
SamplesHG02182
Known GenesUSP54
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3623814
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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