A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4005751



Internal ID22067382
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:10489595..10515370hg38UCSC Ensembl
Outerchr11:10485237..10518796hg38UCSC Ensembl
Innerchr11:10511142..10536917hg19UCSC Ensembl
Outerchr11:10506784..10540343hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3833560
hg1933560
Variant TypeCNV duplication
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1154693
Supporting Variants
Samples
Known GenesAMPD3, MIR4485, MTRNR2L8, RNF141
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4005751
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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