A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25791175



Internal ID19174707
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:176895386..176985584hg38UCSC Ensembl
Innerchr3:176613174..176703372hg19UCSC Ensembl
Innerchr3:178095868..178186066hg18UCSC Ensembl
Cytoband3q26.32
Allele length
AssemblyAllele length
hg3890199
hg1990199
hg1890199
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3893825
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=33
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25791175
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