A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25800220



Internal ID19167342
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:110400024..110415044hg38UCSC Ensembl
Innerchr9:113162304..113177324hg19UCSC Ensembl
Innerchr9:112202125..112217145hg18UCSC Ensembl
Cytoband9q31.3
Allele length
AssemblyAllele length
hg3815021
hg1915021
hg1815021
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891709
Supporting Variants
Samples
Known GenesSVEP1
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=8
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25800220
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