A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25782421



Internal ID19174169
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:31215244..31264081hg38UCSC Ensembl
Innerchr9:31215242..31264079hg19UCSC Ensembl
Innerchr9:31205242..31254079hg18UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg3848838
hg1948838
hg1848838
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891655
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=9
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25782421
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer