A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv606041



Internal ID16393450
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:7292690..7386033hg38UCSC Ensembl
Innerchr7:7332321..7425664hg19UCSC Ensembl
Innerchr7:7298846..7392189hg18UCSC Ensembl
Cytoband7p21.3
Allele length
AssemblyAllele length
hg3893344
hg1993344
hg1893344
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1078879
Samples
Known GenesCOL28A1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv606041
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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