A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv893991



Internal ID6301002
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:134353724..134448296hg19UCSC Ensembl
Outerchr9:134342938..134449467hg19UCSC Ensembl
Innerchr9:133343545..133438117hg18UCSC Ensembl
Outerchr9:133332759..133439288hg18UCSC Ensembl
Cytoband9q34.13
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
Variant TypeCNV Loss
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusS
Merged Variants
Supporting Variantsnssv1585898
SamplesIS37646
Known GenesPOMT1, PRRC2B, SNORD62A, SNORD62B, UCK1
Method
Analysis
PlatformIllumina HumanHap 610 Quad + Illumina HumanHap 1MduoV3
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)nsv893991
Frequency
Sample Size6533
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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