A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6179825



Internal ID9482310
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:19143056..19156984hg38UCSC Ensembl
chr9:19143054..19156982hg19UCSC Ensembl
Cytoband9p22.1
Allele length
AssemblyAllele length
hg3813929
hg1913929
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2661551
Supporting Variants
SamplesNA18952
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6179825
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