A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2660956



Internal ID9580375
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:78970455..78970904hg38UCSC Ensembl
chr15:79262797..79263246hg19UCSC Ensembl
Cytoband15q25.1
Allele length
AssemblyAllele length
hg38450
hg19450
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6284328, essv6409226, essv5475178, essv6200256, essv5486273, essv6142811
SamplesHG00689, HG00683, NA19070, NA18576, HG00174, NA19346
Known GenesRASGRF1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2660956
Frequency
Sample Size1151
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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