A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3623694



Internal ID7010550
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:67784938..67795564hg38UCSC Ensembl
Innerchr10:67785088..67795414hg38UCSC Ensembl
Outerchr10:67784788..67795714hg38UCSC Ensembl
chr10:69544696..69555322hg19UCSC Ensembl
Innerchr10:69544846..69555172hg19UCSC Ensembl
Outerchr10:69544546..69555472hg19UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg3810627
hg1910627
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13848631
SamplesHG00732
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3623694
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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