A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6131214



Internal ID9530166
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:130838503..130840492hg38UCSC Ensembl
chr8:131850749..131852738hg19UCSC Ensembl
Cytoband8q24.22
Allele length
AssemblyAllele length
hg381990
hg191990
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2675868
Supporting Variants
SamplesNA19059
Known GenesADCY8
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6131214
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