A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv452660



Internal ID18274254
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:30175777..30726259hg38UCSC Ensembl
Innerchr15:30467980..31018462hg19UCSC Ensembl
Innerchr15:28255272..28805754hg18UCSC Ensembl
Cytoband15q13.2
Allele length
AssemblyAllele length
hg38550483
hg19550483
hg18550483
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv428300
Supporting Variants
SamplesHGDP01089
Known GenesARHGAP11B, CHRFAM7A, DKFZP434L187, GOLGA8H, LOC100288637, LOC101059918, ULK4P1, ULK4P2
MethodBAC aCGH
AnalysisCopy number variable segments were automatically detected using the CNVfinder algorithm (Fiegler et al. 2006).
PlatformSanger H. sapiens Whole Genome Tile Path 28.7k v3
Comments
ReferencePerry_et_al_2008b
Pubmed ID18775914
Accession Number(s)nssv452660
Frequency
Sample Size62
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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