A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv601939



Internal ID16042662
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:31490856..31504682hg38UCSC Ensembl
Innerchr6:31458633..31472459hg19UCSC Ensembl
Innerchr6:31566612..31580438hg18UCSC Ensembl
Cytoband6p21.33
Allele length
AssemblyAllele length
hg3813827
hg1913827
hg1813827
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10460n54
Supporting Variantsnssv1053521
Samples
Known GenesMICB
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv601939
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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