A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv601119



Internal ID16041842
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:22274537..22417600hg38UCSC Ensembl
Innerchr6:22274766..22417829hg19UCSC Ensembl
Innerchr6:22382745..22525808hg18UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg38143064
hg19143064
hg18143064
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1051098
Samples
Known GenesPRL
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv601119
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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