A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5909783



Internal ID8887186
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:162313496..162323202hg38UCSC Ensembl
chr6:162734528..162744234hg19UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg389707
hg199707
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2676221
Supporting Variants
SamplesNA18534
Known GenesPARK2
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5909783
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