A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv592765



Internal ID16380174
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:189646635..189648974hg38UCSC Ensembl
Innerchr3:189364424..189366763hg19UCSC Ensembl
Innerchr3:190847118..190849457hg18UCSC Ensembl
Cytoband3q28
Allele length
AssemblyAllele length
hg382340
hg192340
hg182340
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv982908, nssv982911, nssv982912, nssv982910, nssv982914, nssv982915, nssv982909, nssv982918, nssv982916, nssv982913, nssv982917
Samples
Known GenesTP63
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv592765
Frequency
Sample Size17421
Observed Gain0
Observed Loss11
Observed Complex0
Frequencyn/a


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