A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv824818



Internal ID6137858
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:2146861..2154396hg19UCSC Ensembl
Innerchr9:2136861..2144396hg18UCSC Ensembl
Cytoband9p24.3
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
Variant TypeCNV Loss
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusS
Merged Variants
Supporting Variantsnssv1431460
SamplesAK18
Known GenesSMARCA2
Method
AnalysisIdentical to variant call (no regions submitted)
PlatformAgilent 24M aCGH
Comments
ReferencePark_et_al_2010
Pubmed ID20364138
Accession Number(s)nsv824818
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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