A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv591713



Internal ID16379122
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:130413146..130414007hg38UCSC Ensembl
Innerchr3:130131990..130132851hg19UCSC Ensembl
Innerchr3:131614680..131615541hg18UCSC Ensembl
Cytoband3q22.1
Allele length
AssemblyAllele length
hg38862
hg19862
hg18862
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8589n54
Supporting Variantsnssv973524, nssv973523
Samples
Known GenesCOL6A5
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv591713
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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