A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13715488



Internal ID1021709
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3622593
Supporting Variants
SamplesHG00640
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13715488
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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