A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2995920



Internal ID15234780
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:44901043..45067965hg38UCSC Ensembl
Innerchr11:44922594..45089516hg19UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg38166923
hg19166923
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv482977
Supporting Variants
Samples
Known GenesLOC221122, TP53I11, TSPAN18
MethodBAC aCGH
Analysis
PlatformSpectral Genomics 2600 BAC array
Comments
ReferenceIafrate_et_al_2004
Pubmed ID15286789
Accession Number(s)nssv2995920
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