A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv452744



Internal ID18273348
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:74078976..74172575hg38UCSC Ensembl
Innerchr15:74371317..74464916hg19UCSC Ensembl
Innerchr15:72158370..72251969hg18UCSC Ensembl
Cytoband15q24.1
Allele length
AssemblyAllele length
hg3893600
hg1993600
hg1893600
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv428308
Supporting Variants
SamplesHGDP00463
Known GenesGOLGA6A, ISLR2, LOC283731
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)nssv452744
Frequency
Sample Size62
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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