A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv589723



Internal ID16377132
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:13034463..13094075hg38UCSC Ensembl
Innerchr3:13075963..13135575hg19UCSC Ensembl
Innerchr3:13050963..13110575hg18UCSC Ensembl
Cytoband3p25.1
Allele length
AssemblyAllele length
hg3859613
hg1959613
hg1859613
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8228n54
Supporting Variantsnssv959135
Samples
Known GenesIQSEC1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv589723
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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