A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv830627



Internal ID6156351
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:31496214..31659950hg19UCSC Ensembl
Outerchr6:31604193..31767929hg18UCSC Ensembl
Outerchr6:31604193..31767929hg17UCSC Ensembl
Cytoband6p21.33
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 Variantsnssv1445322
Samples
Known GenesABHD16A, AIF1, APOM, ATP6V1G2, ATP6V1G2-DDX39B, BAG6, C6orf47, CSNK2B, DDX39B, GPANK1, LST1, LTA, LTB, LY6G5B, LY6G5C, MCCD1, NCR3, NFKBIL1, PRRC2A, SNORA38, SNORD117, SNORD84, TNF
Method
Analysis
PlatformSMRT Whole Genome Tile Path BAC CGH Array
Comments
ReferenceWong_et_al_2007
Pubmed ID17160897
Accession Number(s)nsv830627
Frequency
Sample Size95
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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