A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv603482



Internal ID16390891
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:66242935..66693698hg38UCSC Ensembl
Innerchr6:66952828..67403591hg19UCSC Ensembl
Innerchr6:67009549..67460312hg18UCSC Ensembl
Cytoband6q12
Allele length
AssemblyAllele length
hg38450764
hg19450764
hg18450764
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10734n54
Supporting Variantsnssv1062726
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv603482
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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