A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv892074



Internal ID6299085
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:2623698..2629460hg19UCSC Ensembl
Outerchr9:2623615..2629776hg19UCSC Ensembl
Innerchr9:2613698..2619460hg18UCSC Ensembl
Outerchr9:2613615..2619776hg18UCSC Ensembl
Cytoband9p24.2
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
Variant TypeCNV Loss
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusS
Merged Variants
Supporting Variantsnssv1506593
SamplesSP54381
Known GenesVLDLR
Method
Analysis
PlatformIllumina HumanHap 610 Quad + Illumina HumanHap 1MduoV3
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)nsv892074
Frequency
Sample Size6533
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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