A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3623697



Internal ID7010553
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:67974174..68109985hg38UCSC Ensembl
chr10:69733931..69869742hg19UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg38135812
hg19135812
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13848635
SamplesHG03914
Known GenesHERC4, MYPN
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3623697
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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