A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6168073



Internal ID9145476
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:162296936..162330305hg38UCSC Ensembl
Outerchr6:162296902..162330340hg38UCSC Ensembl
Innerchr6:162717968..162751337hg19UCSC Ensembl
Outerchr6:162717934..162751372hg19UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg3833439
hg1933439
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2664127
Supporting Variants
SamplesNA19448
Known GenesPARK2
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6168073
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