A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25789263



Internal ID18825891
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:8955377..8984503hg38UCSC Ensembl
Innerchr1:9015436..9044562hg19UCSC Ensembl
Innerchr1:8938023..8967149hg18UCSC Ensembl
Cytoband1p36.23
Allele length
AssemblyAllele length
hg3829127
hg1929127
hg1829127
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3890637
Supporting Variants
Samples
Known GenesCA6
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=13
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25789263
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