A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv428242



Internal ID18278006
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:130607951..131583141hg38UCSC Ensembl
Innerchr10:132406215..133381404hg19UCSC Ensembl
Innerchr10:132296205..133271394hg18UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg38975191
hg19975190
hg18975190
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv451982
SamplesHGDP00450
Known GenesMIR378C, TCERG1L
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)nsv428242
Frequency
Sample Size62
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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