A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv452685



Internal ID18273182
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:34306400..34618976hg38UCSC Ensembl
Innerchr15:34598601..34911177hg19UCSC Ensembl
Innerchr15:32385893..32698469hg18UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg38312577
hg19312577
hg18312577
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv428303
Supporting Variants
SamplesHGDP00460
Known GenesGOLGA8A, GOLGA8B, LPCAT4, MIR1233-1, MIR1233-2, NOP10, NUTM1, SLC12A6
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)nssv452685
Frequency
Sample Size62
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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