A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2996372



Internal ID15235232
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:10171748..10331433hg38UCSC Ensembl
Innerchr11:10193295..10352980hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg38159686
hg19159686
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv483076
Supporting Variants
Samples
Known GenesADM, CAND1.11, SBF2
MethodBAC aCGH
Analysis
PlatformSpectral Genomics 2600 BAC array
Comments
ReferenceIafrate_et_al_2004
Pubmed ID15286789
Accession Number(s)nssv2996372
Frequency
Sample Size39
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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