A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5859960



Internal ID22634895
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:81275122..81284186hg38UCSC Ensembl
chr14:81741466..81750530hg19UCSC Ensembl
Cytoband14q31.1
Allele length
AssemblyAllele length
hg389065
hg199065
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17463247
Samples
Known GenesSTON2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5859960
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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