A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv451307



Internal ID18273283
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:143450682..143870527hg38UCSC Ensembl
Innerchr7:143147775..143567620hg19UCSC Ensembl
Innerchr7:142857897..143198553hg18UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg38419846
hg19419846
hg18340657
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv428188
Supporting Variants
SamplesHGDP00462
Known GenesCTAGE15, CTAGE6, EPHA1-AS1, FAM115A, FAM115C, LOC154761, 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)nssv451307
Frequency
Sample Size62
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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