A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3623249



Internal ID7010106
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:52555277..52670314hg38UCSC Ensembl
chr10:54315037..54430074hg19UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg38115038
hg19115038
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13807119
SamplesNA18749
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3623249
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer