A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6144792



Internal ID9122195
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:9188763..9189244hg38UCSC Ensembl
chr20:9169410..9169891hg19UCSC Ensembl
Cytoband20p12.3
Allele length
AssemblyAllele length
hg38482
hg19482
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2660714
Supporting Variants
SamplesNA18596
Known GenesPLCB4
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6144792
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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