A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3624153



Internal ID7011009
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:89148338..89168553hg38UCSC Ensembl
Innerchr10:89148338..89168553hg38UCSC Ensembl
Outerchr10:89147838..89169053hg38UCSC Ensembl
chr10:90908095..90928310hg19UCSC Ensembl
Innerchr10:90908095..90928310hg19UCSC Ensembl
Outerchr10:90907595..90928810hg19UCSC Ensembl
Cytoband10q23.31
Allele length
AssemblyAllele length
hg3820216
hg1920216
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13890582
SamplesHG01977
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3624153
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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