A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6149570



Internal ID9126973
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:288332..289180hg38UCSC Ensembl
chr3:330015..330863hg19UCSC Ensembl
Cytoband3p26.3
Allele length
AssemblyAllele length
hg38849
hg19849
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2662179
Supporting Variants
SamplesNA19399
Known GenesCHL1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6149570
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