A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv894434



Internal ID6301445
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:139552461..139590934hg19UCSC Ensembl
Outerchr9:139544437..139596420hg19UCSC Ensembl
Innerchr9:138672282..138710755hg18UCSC Ensembl
Outerchr9:138664258..138716241hg18UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
Variant TypeCNV Loss
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusS
Merged Variants
Supporting Variantsnssv1509334
SamplesSP54782
Known GenesAGPAT2, EGFL7, MIR126
Method
Analysis
PlatformIllumina HumanHap 610 Quad + Illumina HumanHap 1MduoV3
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)nsv894434
Frequency
Sample Size6533
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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