A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3622823



Internal ID7009681
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:31985116..31996140hg38UCSC Ensembl
chr10:32274044..32285068hg19UCSC Ensembl
Cytoband10p11.22
Allele length
AssemblyAllele length
hg3811025
hg1911025
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv107e214
Supporting Variantsessv13749849
SamplesHG01122
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3622823
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