A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3611492



Internal ID6651710
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:162140792..162286626hg38UCSC Ensembl
chr6:162561824..162707658hg19UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg38145835
hg19145835
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12620272, essv12620273, essv12620274, essv12620275, essv12620271
SamplesHG00182, NA19059, HG00372, HG03717, HG03740
Known GenesPARK2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3611492
Frequency
Sample Size2504
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer