A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1156191



Internal ID22086696
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:80217724..80242935hg38UCSC Ensembl
Outerchr4:80214595..80248354hg38UCSC Ensembl
Innerchr4:81138878..81164089hg19UCSC Ensembl
Outerchr4:81135749..81169508hg19UCSC Ensembl
Cytoband4q21.21
Allele length
AssemblyAllele length
hg3833760
hg1933760
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4014710
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1156191
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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