A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv452591



Internal ID18273505
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:22289962..22734426hg19UCSC Ensembl
Innerchr15:19791326..20285790hg18UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg19444465
hg18494465
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv428296
Supporting Variants
SamplesHGDP00471
Known GenesGOLGA8DP, LOC727924, MIR4509-1, MIR4509-2, MIR4509-3, OR4M2, OR4N3P, OR4N4, REREP3
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)nssv452591
Frequency
Sample Size62
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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