A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1145389



Internal ID15651889
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:133071778..133082065hg38UCSC Ensembl
Innerchr9:135947165..135957452hg19UCSC Ensembl
Innerchr9:134936986..134947273hg18UCSC Ensembl
Cytoband9q34.2
Allele length
AssemblyAllele length
hg3810288
hg1910288
hg1810288
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv615601
Supporting Variants
Samples
Known GenesCEL
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1145389
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