A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1155009



Internal ID22085514
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:21582009..21587633hg38UCSC Ensembl
Outerchr14:21580443..21603051hg38UCSC Ensembl
Innerchr14:22050143..22055757hg19UCSC Ensembl
Outerchr14:22048577..22071202hg19UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg3822609
hg1922626
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4009411
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1155009
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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