A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv452833



Internal ID18273557
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:84389948..84696426hg38UCSC Ensembl
Innerchr15:84944646..85239657hg19UCSC Ensembl
Innerchr15:82735650..83040661hg18UCSC Ensembl
Cytoband15q25.2
Allele length
AssemblyAllele length
hg38306479
hg19295012
hg18305012
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv428310
Supporting Variants
SamplesHGDP00472
Known GenesDNM1P41, GOLGA6L5P, LINC00933, NMB, SCAND2P, SEC11A, UBE2Q2P1, WDR73, ZSCAN2
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)nssv452833
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