A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv428158



Internal ID5947818
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:170581751..171009919hg19UCSC Ensembl
Innerchr6:170423676..170851844hg18UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
Variant TypeCNV Gain
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Merged StatusM
Merged Variants
Supporting Variantsnssv450895, nssv450896
SamplesNA19096, NA19181
Known GenesDLL1, FAM120B, MIR4644, PDCD2, PSMB1, TBP
Method
AnalysisCNVRs were generated by merging all individual human CNV calls.
PlatformSanger H. sapiens Whole Genome Tile Path 28.7k v3
Comments
ReferencePerry et al 2008b
Pubmed ID18775914
Accession Number(s)nsv428158
Frequency
Sample Size62
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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