A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv832323



Internal ID6158047
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr12:6771399..6965723hg19UCSC Ensembl
Outerchr12:6641660..6835984hg18UCSC Ensembl
Outerchr12:6641660..6835984hg17UCSC Ensembl
Cytoband12p13.31
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
hg17n/a
Variant TypeCNV Loss
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusS
Merged Variants
Supporting Variantsnssv1449583
Samples
Known GenesC12orf53, CD4, CDCA3, COPS7A, GNB3, GPR162, ING4, LAG3, LEPREL2, MLF2, PTMS, USP5, ZNF384
Method
Analysis
PlatformSMRT Whole Genome Tile Path BAC CGH Array
Comments
ReferenceWong_et_al_2007
Pubmed ID17160897
Accession Number(s)nsv832323
Frequency
Sample Size95
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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