A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv601341



Internal ID16042064
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:29893694..29906838hg38UCSC Ensembl
Innerchr6:29861471..29874615hg19UCSC Ensembl
Innerchr6:29969450..29982594hg18UCSC Ensembl
Cytoband6p21.33
Allele length
AssemblyAllele length
hg3813145
hg1913145
hg1813145
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10351n54
Supporting Variantsnssv1051990, nssv1051989, nssv1051988
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv601341
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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