A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3620772



Internal ID7007642
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:77384232..77401661hg38UCSC Ensembl
chr9:79999148..80016577hg19UCSC Ensembl
Cytoband9q21.2
Allele length
AssemblyAllele length
hg3817430
hg1917430
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13531845
SamplesNA20897
Known GenesVPS13A
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3620772
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