A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25783521



Internal ID19164652
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:7668843..7735283hg38UCSC Ensembl
Innerchr9:7668843..7735283hg19UCSC Ensembl
Innerchr9:7658843..7725283hg18UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg3866441
hg1966441
hg1866441
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891550
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=27
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25783521
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