A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1156012



Internal ID22086517
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:119632551..119635091hg38UCSC Ensembl
Outerchr3:119631498..119636564hg38UCSC Ensembl
Innerchr3:119351398..119353938hg19UCSC Ensembl
Outerchr3:119350345..119355411hg19UCSC Ensembl
Cytoband3q13.33
Allele length
AssemblyAllele length
hg385067
hg195067
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4017822, nssv4017824, nssv4017823, nssv4017821
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1156012
Frequency
Sample Size131
Observed Gain1
Observed Loss3
Observed Complex0
Frequencyn/a


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