A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3623695



Internal ID6663862
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:67789569..67799780hg38UCSC Ensembl
Innerchr10:67789569..67799780hg38UCSC Ensembl
Outerchr10:67789476..67800004hg38UCSC Ensembl
chr10:69549327..69559538hg19UCSC Ensembl
Innerchr10:69549327..69559538hg19UCSC Ensembl
Outerchr10:69549234..69559762hg19UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg3810212
hg1910212
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13848632, essv13848633
SamplesHG00732, NA19064
Known GenesDNAJC12
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3623695
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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