A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6490324



Internal ID9660598
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:34904642..34905658hg38UCSC Ensembl
chr15:35196843..35197859hg19UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg381017
hg191017
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2668318
Supporting Variants
SamplesNA19393
Known GenesAQR
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6490324
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