A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv825350



Internal ID6138390
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:43592969..43593651hg19UCSC Ensembl
Innerchr10:42912975..42913657hg18UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
Variant TypeCNV Gain
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusS
Merged Variants
Supporting Variantsnssv1441276
SamplesNA18969
Known GenesRET
Method
AnalysisIdentical to variant call (no regions submitted)
PlatformAgilent 24M aCGH
Comments
ReferencePark_et_al_2010
Pubmed ID20364138
Accession Number(s)nsv825350
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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