A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv450912



Internal ID18275041
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:13709..203581hg38UCSC Ensembl
Innerchr7:13709..203581hg19UCSC Ensembl
Innerchr7:106471..298664hg18UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg38189873
hg19189873
hg18192194
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv428159
Supporting Variants
SamplesNA19181
Known GenesFAM20C, LOC100507642
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)nssv450912
Frequency
Sample Size62
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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