A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv604390



Internal ID16391799
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:104404549..104424941hg38UCSC Ensembl
Innerchr6:104852424..104872816hg19UCSC Ensembl
Innerchr6:104959117..104979509hg18UCSC Ensembl
Cytoband6q16.3
Allele length
AssemblyAllele length
hg3820393
hg1920393
hg1820393
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1071656
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv604390
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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