A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5444439



Internal ID8421842
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:78791921..78792013hg38UCSC Ensembl
chr15:79084263..79084355hg19UCSC Ensembl
Cytoband15q25.1
Allele length
AssemblyAllele length
hg3893
hg1993
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2665394
Supporting Variants
SamplesHG01519
Known GenesADAMTS7
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5444439
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