A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25782628



Internal ID19174220
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:4895947..4911930hg38UCSC Ensembl
Innerchr9:4895947..4911930hg19UCSC Ensembl
Innerchr9:4885947..4901930hg18UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg3815984
hg1915984
hg1815984
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891534
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=8
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25782628
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