A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv569e214



Internal ID20121992
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:35183869..35195954hg38UCSC Ensembl
chr17:33510888..33522973hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg3812086
hg1912086
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3640441, esv3640440
SamplesNA19917, HG03708, HG03642, HG00628
Known GenesSLC35G3, UNC45B
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)dgv569e214
Frequency
Sample Size2504
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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