A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv890625



Internal ID6297636
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:19371767..19784574hg19UCSC Ensembl
Outerchr8:19368697..19799641hg19UCSC Ensembl
Innerchr8:19416047..19828854hg18UCSC Ensembl
Outerchr8:19412977..19843921hg18UCSC Ensembl
Cytoband8p21.3
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
Variant TypeCNV Gain
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusS
Merged Variants
Supporting Variantsnssv1549014
SamplesMS17974
Known GenesCSGALNACT1, INTS10, LPL
Method
Analysis
PlatformIllumina HumanHap 610 Quad + Illumina HumanHap 1MduoV3
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)nsv890625
Frequency
Sample Size6533
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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