A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13861550



Internal ID3863366
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3623787
Supporting Variants
SamplesNA19443
Known GenesCHST3
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13861550
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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