A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv453290



Internal ID18273192
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:89872941..90185980hg38UCSC Ensembl
Innerchr16:89939349..90252388hg19UCSC Ensembl
Innerchr16:88466850..88779889hg18UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg38313040
hg19313040
hg18313040
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv428331
Supporting Variants
SamplesHGDP00460
Known GenesAFG3L1P, C16orf3, CENPBD1, DBNDD1, DEF8, GAS8, MC1R, PRDM7, TCF25, TUBB3, URAHP
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)nssv453290
Frequency
Sample Size62
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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