A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv893926



Internal ID6300937
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:132425233..132501881hg19UCSC Ensembl
Outerchr9:132420439..132502430hg19UCSC Ensembl
Innerchr9:131465054..131541702hg18UCSC Ensembl
Outerchr9:131460260..131542251hg18UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
Variant TypeCNV Gain
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusS
Merged Variants
Supporting Variantsnssv1587125
SamplesIS37986
Known GenesPRRX2, PTGES
Method
Analysis
PlatformIllumina HumanHap 610 Quad + Illumina HumanHap 1MduoV3
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)nsv893926
Frequency
Sample Size6533
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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