A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv824819



Internal ID6137859
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:2620547..2623694hg19UCSC Ensembl
Innerchr9:2610547..2613694hg18UCSC Ensembl
Cytoband9p24.2
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
Variant TypeCNV Gain
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusS
Merged Variants
Supporting Variantsnssv1441407
SamplesNA18547
Known GenesFLJ35024, VLDLR
Method
AnalysisIdentical to variant call (no regions submitted)
PlatformAgilent 24M aCGH
Comments
ReferencePark_et_al_2010
Pubmed ID20364138
Accession Number(s)nsv824819
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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