A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1155025



Internal ID22085530
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:54153930..54160852hg38UCSC Ensembl
Outerchr14:54151676..54164713hg38UCSC Ensembl
Innerchr14:54620648..54627570hg19UCSC Ensembl
Outerchr14:54618394..54631431hg19UCSC Ensembl
Cytoband14q22.2
Allele length
AssemblyAllele length
hg3813038
hg1913038
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4009462
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1155025
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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