A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv892075



Internal ID6299086
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:2645201..2651714hg19UCSC Ensembl
Outerchr9:2645109..2651809hg19UCSC Ensembl
Innerchr9:2635201..2641714hg18UCSC Ensembl
Outerchr9:2635109..2641809hg18UCSC 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 Variantsnssv1504696
SamplesSP52708
Known GenesVLDLR
Method
Analysis
PlatformIllumina HumanHap 610 Quad + Illumina HumanHap 1MduoV3
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)nsv892075
Frequency
Sample Size6533
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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