A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5902868



Internal ID8880271
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:162157519..162159247hg38UCSC Ensembl
chr6:162578551..162580279hg19UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg381729
hg191729
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2662124
Supporting Variants
SamplesNA19371
Known GenesPARK2
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5902868
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