A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv428136



Internal ID5948460
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:15595640..15781241hg19UCSC Ensembl
Innerchr6:15703619..15889220hg18UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
Variant TypeCNV Gain
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Merged StatusS
Merged Variants
Supporting Variantsnssv450608
SamplesNA19189
Known GenesDTNBP1
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)nsv428136
Frequency
Sample Size62
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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