A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv592009



Internal ID16379418
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:149550714..149551571hg38UCSC Ensembl
Innerchr3:149268501..149269358hg19UCSC Ensembl
Innerchr3:150751191..150752048hg18UCSC Ensembl
Cytoband3q25.1
Allele length
AssemblyAllele length
hg38858
hg19858
hg18858
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8644n54
Supporting Variantsnssv976518, nssv976520, nssv976519
Samples
Known GenesWWTR1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv592009
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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