A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13860918



Internal ID3348416
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:71876896..71877412hg38UCSC Ensembl
Innerchr10:71876898..71877410hg38UCSC Ensembl
Outerchr10:71876894..71877414hg38UCSC Ensembl
chr10:73636654..73637170hg19UCSC Ensembl
Innerchr10:73636656..73637168hg19UCSC Ensembl
Outerchr10:73636652..73637172hg19UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg38517
hg19517
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3623782
Supporting Variants
SamplesHG02983
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13860918
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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