A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5853450



Internal ID22628385
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:81422759..81424208hg38UCSC Ensembl
chr14:81889103..81890552hg19UCSC Ensembl
Cytoband14q31.1
Allele length
AssemblyAllele length
hg381450
hg191450
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17469228
Samples
Known GenesSTON2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5853450
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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