A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5867096



Internal ID22642031
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:32964761..32974347hg38UCSC Ensembl
chr14:33433967..33443553hg19UCSC Ensembl
Cytoband14q13.1
Allele length
AssemblyAllele length
hg389587
hg199587
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17461107
Samples
Known GenesNPAS3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5867096
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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