A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2558n100



Internal ID20154174
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:34403109..34538731hg38UCSC Ensembl
chr15:34695310..34830932hg19UCSC Ensembl
chr15:32482602..32618224hg18UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg38135623
hg19135623
hg18135623
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1053288, nsv1039585, nsv1046628, nsv1038843, nsv1052868, nsv1035788, nsv1051208
Samples
Known GenesGOLGA8A, GOLGA8B, MIR1233-1, MIR1233-2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv2558n100
Frequency
Sample Size29084
Observed Gain25
Observed Loss156
Observed Complex0
Frequencyn/a


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