A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv450895



Internal ID18275043
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:170272663..170535221hg38UCSC Ensembl
Innerchr6:170581751..170844309hg19UCSC Ensembl
Innerchr6:170423676..170686234hg18UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg38262559
hg19262559
hg18262559
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv428158
Supporting Variants
SamplesNA19181
Known GenesDLL1, FAM120B, FLJ38122, MIR4644, PSMB1
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)nssv450895
Frequency
Sample Size62
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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