A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv589722



Internal ID16377131
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:13029299..13089801hg38UCSC Ensembl
Innerchr3:13070799..13131301hg19UCSC Ensembl
Innerchr3:13045799..13106301hg18UCSC Ensembl
Cytoband3p25.1
Allele length
AssemblyAllele length
hg3860503
hg1960503
hg1860503
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8228n54
Supporting Variantsnssv959134
Samples
Known GenesIQSEC1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv589722
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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