A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1236e214



Internal ID20122659
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:162471174..162499352hg38UCSC Ensembl
chr6:162892206..162920384hg19UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg3828179
hg1928179
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3611538, esv3611536
SamplesHG02272, NA20503, HG01051, HG00593, HG02182, HG01323
Known GenesPARK2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)dgv1236e214
Frequency
Sample Size2504
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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