A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv893909



Internal ID6300920
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:131920181..132489353hg19UCSC Ensembl
Outerchr9:131909736..132496639hg19UCSC Ensembl
Innerchr9:130960002..131529174hg18UCSC Ensembl
Outerchr9:130949557..131536460hg18UCSC 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 Variantsnssv1529825
SamplesMS10123
Known GenesASB6, C9orf106, C9orf50, IER5L, LOC100506190, METTL11A, PPP2R4, PRRX2
Method
Analysis
PlatformIllumina HumanHap 610 Quad + Illumina HumanHap 1MduoV3
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)nsv893909
Frequency
Sample Size6533
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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