A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3620308



Internal ID7007179
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:32716372..32735734hg38UCSC Ensembl
chr9:32716370..32735732hg19UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg3819363
hg1919363
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1471e214
Supporting Variantsessv13451392
SamplesHG02798
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3620308
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