A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3623895



Internal ID7010751
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:78625890..78636485hg38UCSC Ensembl
Innerchr10:78625890..78636485hg38UCSC Ensembl
Outerchr10:78625653..78636721hg38UCSC Ensembl
chr10:80385647..80396242hg19UCSC Ensembl
Innerchr10:80385647..80396242hg19UCSC Ensembl
Outerchr10:80385410..80396478hg19UCSC Ensembl
Cytoband10q22.3
Allele length
AssemblyAllele length
hg3810596
hg1910596
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13866676
SamplesNA19068
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3623895
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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