A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1148286



Internal ID15654786
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:135924406..135992854hg38UCSC Ensembl
Innerchr9:138816252..138884700hg19UCSC Ensembl
Innerchr9:137956073..138024521hg18UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg3868449
hg1968449
hg1868449
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv615945
Supporting Variants
Samples
Known GenesUBAC1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1148286
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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