A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1155035



Internal ID22085540
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:76984765..76995358hg38UCSC Ensembl
Outerchr14:76968708..76996791hg38UCSC Ensembl
Innerchr14:77451108..77461701hg19UCSC Ensembl
Outerchr14:77435051..77463134hg19UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg3828084
hg1928084
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4009703
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1155035
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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