A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3623787



Internal ID6663954
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:71978793..71981003hg38UCSC Ensembl
Innerchr10:71978943..71980853hg38UCSC Ensembl
Outerchr10:71978643..71981153hg38UCSC Ensembl
chr10:73738551..73740761hg19UCSC Ensembl
Innerchr10:73738701..73740611hg19UCSC Ensembl
Outerchr10:73738401..73740911hg19UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg382211
hg192211
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13861550
SamplesNA19443
Known GenesCHST3
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3623787
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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