A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3623705



Internal ID6663872
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:68099008..68297411hg38UCSC Ensembl
chr10:69858765..70057168hg19UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg38198404
hg19198404
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13848748
SamplesHG03914
Known GenesATOH7, MYPN, PBLD
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3623705
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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