A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25789091



Internal ID19164134
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:817186..848643hg38UCSC Ensembl
Innerchr1:752566..784023hg19UCSC Ensembl
Innerchr1:742429..773886hg18UCSC Ensembl
Cytoband1p36.33
Allele length
AssemblyAllele length
hg3831458
hg1931458
hg1831458
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3890635
Supporting Variants
Samples
Known GenesFAM87B, LINC00115, LINC01128
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=10
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25789091
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