A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv451317



Internal ID18274364
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:143450682..143965323hg38UCSC Ensembl
Innerchr7:143147775..143662416hg19UCSC Ensembl
Innerchr7:142857897..143293349hg18UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg38514642
hg19514642
hg18435453
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv428188
Supporting Variants
SamplesHGDP01094
Known GenesCTAGE15, CTAGE6, EPHA1-AS1, FAM115A, FAM115C, LOC154761, OR2F1, OR2F2, TAS2R41
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)nssv451317
Frequency
Sample Size62
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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