A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv451165



Internal ID18274918
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:97773444..98018717hg38UCSC Ensembl
Innerchr7:97402756..97648029hg19UCSC Ensembl
Innerchr7:97240692..97485965hg18UCSC Ensembl
Cytoband7q21.3
Allele length
AssemblyAllele length
hg38245274
hg19245274
hg18245274
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv428178
Supporting Variants
SamplesNA19113
Known GenesASNS, MGC72080, OCM2
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)nssv451165
Frequency
Sample Size62
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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