A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv884418



Internal ID6291429
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:31526856..31739881hg19UCSC Ensembl
Outerchr6:31525448..31741078hg19UCSC Ensembl
Innerchr6:31634835..31847860hg18UCSC Ensembl
Outerchr6:31633427..31849057hg18UCSC Ensembl
Cytoband6p21.33
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
Variant TypeCNV Gain
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusS
Merged Variants
Supporting Variantsnssv1592626
SamplesIS39243
Known GenesABHD16A, AIF1, APOM, BAG6, C6orf25, C6orf26, C6orf27, C6orf47, CLIC1, CSNK2B, DDAH2, GPANK1, LST1, LTA, LTB, LY6G5B, LY6G5C, LY6G6C, LY6G6D, LY6G6E, LY6G6F, MIR4646, MSH5, MSH5-C6orf26, NCR3, NFKBIL1, PRRC2A, SNORA38, TNF
Method
Analysis
PlatformIllumina HumanHap 610 Quad + Illumina HumanHap 1MduoV3
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)nsv884418
Frequency
Sample Size6533
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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