A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv893452



Internal ID6300463
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:75576214..76318623hg19UCSC Ensembl
Outerchr9:75567287..76320898hg19UCSC Ensembl
Innerchr9:74766034..75508443hg18UCSC Ensembl
Outerchr9:74757107..75510718hg18UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
Variant TypeCNV Gain
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusS
Merged Variants
Supporting Variantsnssv1586996
SamplesIS37986
Known GenesALDH1A1, ANXA1
Method
Analysis
PlatformIllumina HumanHap 610 Quad + Illumina HumanHap 1MduoV3
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)nsv893452
Frequency
Sample Size6533
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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