A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1219e214



Internal ID20122642
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:132754654..132762349hg38UCSC Ensembl
chr6:133075793..133083488hg19UCSC Ensembl
Cytoband6q23.2
Allele length
AssemblyAllele length
hg387696
hg197696
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3610844, esv3610845
SamplesHG03784, HG03786
Known GenesVNN2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)dgv1219e214
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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