A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv109e55



Internal ID20126588
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:31604809..32219354hg38UCSC Ensembl
chr15:31897012..32511555hg19UCSC Ensembl
chr15:29684304..30298847hg18UCSC Ensembl
chr15:29684304..30298847hg17UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg38614546
hg19614544
hg18614544
hg17614544
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv34762, esv34816, esv35123, esv2751532, esv2751530, esv2751531
SamplesNA11830, NA12813, SPC_88, BEC_394, BEC_491, NA10856
Known GenesCHRNA7, OTUD7A
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Affymetrix Mapping 250K Sty2 SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)dgv109e55
Frequency
Sample Size771
Observed Gain25
Observed Loss0
Observed Complex0
Frequencyn/a


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