A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv450693



Internal ID18273681
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:32427643..32518189hg38UCSC Ensembl
Innerchr6:32395420..32485966hg19UCSC Ensembl
Innerchr6:32503398..32593944hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg3890547
hg1990547
hg1890547
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv428142
Supporting Variants
SamplesHGDP00474
Known GenesHLA-DRA, HLA-DRB5
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)nssv450693
Frequency
Sample Size62
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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