A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1155013



Internal ID22085518
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:22625942..22630225hg38UCSC Ensembl
Outerchr14:22623202..22630304hg38UCSC Ensembl
Innerchr14:23094845..23099130hg19UCSC Ensembl
Outerchr14:23092105..23099209hg19UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg387103
hg197105
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4009417
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1155013
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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