A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv451597



Internal ID18274895
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:142632040..142732118hg38UCSC Ensembl
Innerchr8:143713401..143813536hg19UCSC Ensembl
Innerchr8:143710403..143810538hg18UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg38100079
hg19100136
hg18100136
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv428207
Supporting Variants
SamplesNA19113
Known GenesJRK, LOC100288181, LY6K, PSCA, THEM6
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)nssv451597
Frequency
Sample Size62
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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