A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1156345



Internal ID22084821
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:54392935..54398341hg38UCSC Ensembl
Outerchr5:54391815..54399111hg38UCSC Ensembl
Innerchr5:53688765..53694171hg19UCSC Ensembl
Outerchr5:53687645..53694941hg19UCSC Ensembl
Cytoband5q11.2
Allele length
AssemblyAllele length
hg387297
hg197297
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv230n97
Supporting Variantsnssv4017545
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1156345
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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