A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv453819



Internal ID18274385
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:1496135..1611612hg38UCSC Ensembl
Innerchr20:1476781..1592258hg19UCSC Ensembl
Innerchr20:1424781..1540258hg18UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg38115478
hg19115478
hg18115478
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv428374
Supporting Variants
SamplesHGDP01094
Known GenesSIRPB1, SIRPD
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)nssv453819
Frequency
Sample Size62
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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