A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv833380



Internal ID6159104
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr17:17088416..17241206hg19UCSC Ensembl
Outerchr17:17029141..17181931hg18UCSC Ensembl
Outerchr17:17029141..17181931hg17UCSC Ensembl
Cytoband17p11.2
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 Variantsnssv1453131
Samples
Known GenesCOPS3, FLCN, MPRIP, NT5M, PLD6
Method
Analysis
PlatformSMRT Whole Genome Tile Path BAC CGH Array
Comments
ReferenceWong_et_al_2007
Pubmed ID17160897
Accession Number(s)nsv833380
Frequency
Sample Size95
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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