A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1057886



Internal ID15911072
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 StatusS
Merged Variantsnsv602874
Supporting Variants
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)nssv1057886
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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