A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv452835



Internal ID18274585
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:85107707..85341481hg38UCSC Ensembl
Innerchr15:85650938..85884712hg19UCSC Ensembl
Innerchr15:83451942..83685716hg18UCSC Ensembl
Cytoband15q25.3
Allele length
AssemblyAllele length
hg38233775
hg19233775
hg18233775
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv428311
Supporting Variants
SamplesNA18916
Known GenesLOC440300, LOC642423, PDE8A
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)nssv452835
Frequency
Sample Size62
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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