A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv823520



Internal ID6136560
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:92232482..92233325hg19UCSC Ensembl
Innerchr1:92005070..92005913hg18UCSC Ensembl
Cytoband1p22.1
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
Variant TypeCNV Loss
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusM
Merged Variants
Supporting Variantsnssv1430354, nssv1424164, nssv1424747, nssv1421458, nssv1431082
SamplesAK16, AK2, AK18, NA18947, NA18997
Known GenesTGFBR3
Method
AnalysisIdentical calls merged by dbVar staff (no regions submitted)
PlatformAgilent 24M aCGH
Comments
ReferencePark_et_al_2010
Pubmed ID20364138
Accession Number(s)nsv823520
Frequency
Sample Size31
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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