A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3622593



Internal ID7009451
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:22276833..22290779hg38UCSC Ensembl
Innerchr10:22276883..22290729hg38UCSC Ensembl
Outerchr10:22276727..22290885hg38UCSC Ensembl
chr10:22565762..22579708hg19UCSC Ensembl
Innerchr10:22565812..22579658hg19UCSC Ensembl
Outerchr10:22565656..22579814hg19UCSC Ensembl
Cytoband10p12.31
Allele length
AssemblyAllele length
hg3813947
hg1913947
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13715488
SamplesHG00640
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3622593
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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