A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4927n100



Internal ID20156543
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:155758758..155774388hg38UCSC Ensembl
chr3:155476547..155492177hg19UCSC Ensembl
chr3:156959241..156974871hg18UCSC Ensembl
Cytoband3q25.31
Allele length
AssemblyAllele length
hg3815631
hg1915631
hg1815631
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1010726, nsv1004723
Samples
Known GenesC3orf33
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv4927n100
Frequency
Sample Size29084
Observed Gain28
Observed Loss0
Observed Complex0
Frequencyn/a


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