A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5932



Internal ID5086269
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:16995294..17040847hg19UCSC Ensembl
Outerchr10:17035300..17080853hg18UCSC Ensembl
Outerchr10:17035300..17080853hg17UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg196276
hg186276
hg176276
Variant TypeCNV Loss
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Merged StatusS
Merged Variants
Supporting Variantsnssv5239
SamplesNA19129
Known GenesCUBN
Method
AnalysisSample level sites were merged to generate a set of non-redundant variant regions. Two non-redundant inversion variants (chr 2 positions 89438708-89655419 and 89958869-91208466) were corrected from the original publication for coordinates and associated sample-level data.
PlatformCapillary
Comments
ReferenceKidd et al 2008
Pubmed ID18451855
Accession Number(s)nsv5932
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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