A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv428206



Internal ID18624656
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:132482661..132672643hg38UCSC Ensembl
Innerchr8:133494908..133684889hg19UCSC Ensembl
Innerchr8:133564090..133754071hg18UCSC Ensembl
Cytoband8q24.22
Allele length
AssemblyAllele length
hg38189983
hg19189982
hg18189982
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv451589
SamplesHGDP00474
Known GenesHPYR1, LRRC6
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)nsv428206
Frequency
Sample Size62
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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