A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7355n54



Internal ID22775250
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:239400274..239401967hg38UCSC Ensembl
chr2:240321968..240323661hg19UCSC Ensembl
chr2:239986905..239988598hg18UCSC Ensembl
Cytoband2q37.3
Allele length
AssemblyAllele length
hg381694
hg191694
hg181694
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv584787, nsv584788
Samples
Known GenesHDAC4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv7355n54
Frequency
Sample Size17421
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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