A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25793011



Internal ID19175727
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:19745778..19926185hg38UCSC Ensembl
Innerchr14:20213937..20394344hg19UCSC Ensembl
Innerchr14:19283777..19464184hg18UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg38180408
hg19180408
hg18180408
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892451
Supporting Variants
Samples
Known GenesOR4K2, OR4K5, OR4M1, OR4N2, OR4Q3
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=14
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25793011
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