A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv603481



Internal ID16390890
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:66242935..66679582hg38UCSC Ensembl
Innerchr6:66952828..67389475hg19UCSC Ensembl
Innerchr6:67009549..67446196hg18UCSC Ensembl
Cytoband6q12
Allele length
AssemblyAllele length
hg38436648
hg19436648
hg18436648
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10734n54
Supporting Variantsnssv1062725
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv603481
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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