A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv483039



Internal ID15235513
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:32574635..32751321hg38UCSC Ensembl
Innerchr15:32866836..33043522hg19UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg38176687
hg19176687
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2996471
Samples
Known GenesARHGAP11A, GOLGA8R, GREM1, LOC100131315, LOC100996255, SCG5
MethodBAC aCGH
Analysis
PlatformSpectral Genomics 2600 BAC array
Comments
ReferenceIafrate_et_al_2004
Pubmed ID15286789
Accession Number(s)nsv483039
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