A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1233e214



Internal ID20122656
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:162194332..162206991hg38UCSC Ensembl
chr6:162615364..162628023hg19UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg3812660
hg1912660
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3611497, esv3611496
SamplesNA19703, HG03717, HG00182, HG03740, NA19059, HG00372
Known GenesPARK2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)dgv1233e214
Frequency
Sample Size2504
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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