A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3624057



Internal ID7010913
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:84979125..85039811hg38UCSC Ensembl
chr10:86738881..86799567hg19UCSC Ensembl
Cytoband10q23.1
Allele length
AssemblyAllele length
hg3860687
hg1960687
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13882180, essv13882181
SamplesHG01597, HG01516
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3624057
Frequency
Sample Size2504
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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