A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1156304



Internal ID22084780
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:5682419..5715019hg38UCSC Ensembl
Outerchr5:5680920..5717261hg38UCSC Ensembl
Innerchr5:5682532..5715132hg19UCSC Ensembl
Outerchr5:5681033..5717374hg19UCSC Ensembl
Cytoband5p15.32
Allele length
AssemblyAllele length
hg3836342
hg1936342
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv228n97
Supporting Variantsnssv4020621
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1156304
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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