A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv893927



Internal ID6300938
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:132478092..132514889hg19UCSC Ensembl
Outerchr9:132473616..132517501hg19UCSC Ensembl
Innerchr9:131517913..131554710hg18UCSC Ensembl
Outerchr9:131513437..131557322hg18UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
Variant TypeCNV Loss
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusS
Merged Variants
Supporting Variantsnssv1530640
SamplesMS10311
Known GenesPRRX2, PTGES
Method
Analysis
PlatformIllumina HumanHap 610 Quad + Illumina HumanHap 1MduoV3
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)nsv893927
Frequency
Sample Size6533
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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