A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv602874



Internal ID16390283
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:34347507..34350763hg38UCSC Ensembl
Innerchr6:34315284..34318540hg19UCSC Ensembl
Innerchr6:34423262..34426518hg18UCSC Ensembl
Cytoband6p21.31
Allele length
AssemblyAllele length
hg383257
hg193257
hg183257
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10618n54
Supporting Variantsnssv1057886
Samples
Known GenesNUDT3, RPS10-NUDT3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv602874
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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