A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv113e55



Internal ID20126592
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:101496174..101853034hg38UCSC Ensembl
chr15:102036377..102393237hg19UCSC Ensembl
chr15:99853900..100210760hg18UCSC Ensembl
chr15:99853900..100210760hg17UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg38356861
hg19356861
hg18356861
hg17356861
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv2751544, esv2751545
SamplesSPC_100, BEC_594
Known GenesOR4F13P, OR4F15, OR4F6, TARSL2, TM2D3
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)dgv113e55
Frequency
Sample Size771
Observed Gain8
Observed Loss0
Observed Complex0
Frequencyn/a


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