A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv452566



Internal ID18274240
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20850656..22308242hg38UCSC Ensembl
Innerchr15:21055985..22596193hg19UCSC Ensembl
Innerchr15:19320573..20097557hg18UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg381457587
hg191540209
hg18776985
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv428296
Supporting Variants
SamplesHGDP01089
Known GenesCT60, CXADRP2, LOC646214, LOC727924, NF1P2, OR4M2, OR4N3P, OR4N4, POTEB, POTEB2, 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)nssv452566
Frequency
Sample Size62
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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