A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv535e214



Internal ID22756429
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:74581749..74598355hg38UCSC Ensembl
chr16:74615647..74632253hg19UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg3816607
hg1916607
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3639072, esv3639071
SamplesNA18530
Known GenesGLG1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)dgv535e214
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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