A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv450894



Internal ID18622026
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:168482707..168683442hg38UCSC Ensembl
Innerchr6:168883387..169083558hg19UCSC Ensembl
Innerchr6:168626236..168825483hg18UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg38200736
hg19200172
hg18199248
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv428156
Supporting Variants
SamplesNA19257
Known GenesSMOC2
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)nssv450894
Frequency
Sample Size62
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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