A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv893058



Internal ID6300069
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:37390630..37421065hg19UCSC Ensembl
Outerchr9:37387218..37426152hg19UCSC Ensembl
Innerchr9:37380630..37411065hg18UCSC Ensembl
Outerchr9:37377218..37416152hg18UCSC Ensembl
Cytoband9p13.2
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
Variant TypeCNV Gain
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusS
Merged Variants
Supporting Variantsnssv1586980
SamplesIS37986
Known GenesGRHPR
Method
Analysis
PlatformIllumina HumanHap 610 Quad + Illumina HumanHap 1MduoV3
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)nsv893058
Frequency
Sample Size6533
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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