A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv601344



Internal ID16042067
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:29893694..29920722hg38UCSC Ensembl
Innerchr6:29861471..29888499hg19UCSC Ensembl
Innerchr6:29969450..29996478hg18UCSC Ensembl
Cytoband6p21.33
Allele length
AssemblyAllele length
hg3827029
hg1927029
hg1827029
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10346n54
Supporting Variantsnssv1051994
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv601344
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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