A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25781178



Internal ID19167576
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:161562..206255hg38UCSC Ensembl
Innerchr9:161562..206255hg19UCSC Ensembl
Innerchr9:151562..196255hg18UCSC Ensembl
Cytoband9p24.3
Allele length
AssemblyAllele length
hg3844694
hg1944694
hg1844694
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891507
Supporting Variants
Samples
Known GenesCBWD1
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=7
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25781178
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