A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3623050



Internal ID7009907
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:43698136..43706660hg38UCSC Ensembl
chr10:44193584..44202108hg19UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg388525
hg198525
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13764530, essv13764529
SamplesNA19028, NA19377
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3623050
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