A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv833128



Internal ID6158852
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:3575122..3740498hg19UCSC Ensembl
Outerchr16:3515123..3680499hg18UCSC Ensembl
Outerchr16:3515123..3680499hg17UCSC Ensembl
Cytoband16p13.3
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 Variantsnssv1452256
Samples
Known GenesCLUAP1, DNASE1, NLRC3, SLX4, TRAP1
Method
Analysis
PlatformSMRT Whole Genome Tile Path BAC CGH Array
Comments
ReferenceWong_et_al_2007
Pubmed ID17160897
Accession Number(s)nsv833128
Frequency
Sample Size95
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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