A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13866608



Internal ID5713251
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:77934809..77935572hg38UCSC Ensembl
Innerchr10:77934809..77935572hg38UCSC Ensembl
Outerchr10:77934521..77935742hg38UCSC Ensembl
chr10:79694567..79695330hg19UCSC Ensembl
Innerchr10:79694567..79695330hg19UCSC Ensembl
Outerchr10:79694279..79695500hg19UCSC Ensembl
Cytoband10q22.3
Allele length
AssemblyAllele length
hg38764
hg19764
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3623884
Supporting Variants
SamplesNA19095
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13866608
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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