A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3622576



Internal ID7009434
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:21327903..21338106hg38UCSC Ensembl
chr10:21616832..21627035hg19UCSC Ensembl
Cytoband10p12.31
Allele length
AssemblyAllele length
hg3810204
hg1910204
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13715207
SamplesNA19431
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3622576
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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