A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv601349



Internal ID16042072
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:29893749..29907748hg38UCSC Ensembl
Innerchr6:29861526..29875525hg19UCSC Ensembl
Innerchr6:29969505..29983504hg18UCSC Ensembl
Cytoband6p21.33
Allele length
AssemblyAllele length
hg3814000
hg1914000
hg1814000
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10351n54
Supporting Variantsnssv1051999
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv601349
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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