A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25792145



Internal ID18827848
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:32393132..32776080hg38UCSC Ensembl
Innerchr15:32685333..33068281hg19UCSC Ensembl
Innerchr15:30472625..30855573hg18UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg38382949
hg19382949
hg18382949
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892661
Supporting Variants
Samples
Known GenesARHGAP11A, FMN1, GOLGA8K, GOLGA8O, GOLGA8R, GREM1, LOC100131315, LOC100996255, SCG5, ULK4P1, ULK4P2, ULK4P3, WHAMMP1
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=99
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25792145
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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