A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv450848



Internal ID18620215
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:118109354..118265811hg38UCSC Ensembl
Innerchr6:118430517..118586974hg19UCSC Ensembl
Innerchr6:118537210..118693667hg18UCSC Ensembl
Cytoband6q22.2
Allele length
AssemblyAllele length
hg38156458
hg19156458
hg18156458
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv428153
Supporting Variants
SamplesHGDP00471
Known GenesSLC35F1
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)nssv450848
Frequency
Sample Size62
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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