A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv892076



Internal ID6299087
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:2645773..2653450hg19UCSC Ensembl
Outerchr9:2645651..2653719hg19UCSC Ensembl
Innerchr9:2635773..2643450hg18UCSC Ensembl
Outerchr9:2635651..2643719hg18UCSC Ensembl
Cytoband9p24.2
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
Variant TypeCNV Gain
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusS
Merged Variants
Supporting Variantsnssv1503803
SamplesSP52113
Known GenesVLDLR
Method
Analysis
PlatformIllumina HumanHap 610 Quad + Illumina HumanHap 1MduoV3
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)nsv892076
Frequency
Sample Size6533
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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