A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv830567



Internal ID6156291
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr5:180530365..180682322hg19UCSC Ensembl
Outerchr5:180462971..180614928hg18UCSC Ensembl
Outerchr5:180462971..180614928hg17UCSC Ensembl
Cytoband5q35.3
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 Variantsnssv1445180
Samples
Known GenesGNB2L1, MIR4638, OR2V2, SNORD95, SNORD96A, TRIM41, TRIM7
Method
Analysis
PlatformSMRT Whole Genome Tile Path BAC CGH Array
Comments
ReferenceWong_et_al_2007
Pubmed ID17160897
Accession Number(s)nsv830567
Frequency
Sample Size95
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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