A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv893925



Internal ID6300936
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:132414185..132579110hg19UCSC Ensembl
Outerchr9:132412706..132585058hg19UCSC Ensembl
Innerchr9:131454006..131618931hg18UCSC Ensembl
Outerchr9:131452527..131624879hg18UCSC 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 Variantsnssv1537438
SamplesMS13206
Known GenesPRRX2, PTGES, TOR1A, TOR1B
Method
Analysis
PlatformIllumina HumanHap 610 Quad + Illumina HumanHap 1MduoV3
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)nsv893925
Frequency
Sample Size6533
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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