A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25790939



Internal ID18821388
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:130128318..130352524hg38UCSC Ensembl
Innerchr2:130885891..131110097hg19UCSC Ensembl
Innerchr2:130602361..130826567hg18UCSC Ensembl
Cytoband2q21.1
Allele length
AssemblyAllele length
hg38224207
hg19224207
hg18224207
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3893326
Supporting Variants
Samples
Known GenesCCDC115, CCDC74B, IMP4, MED15P9, MZT2B, POTEF, SMPD4, TUBA3E
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=35
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25790939
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