A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5850065



Internal ID22625000
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:94641856..94657460hg38UCSC Ensembl
chr14:95108193..95123797hg19UCSC Ensembl
Cytoband14q32.13
Allele length
AssemblyAllele length
hg3815605
hg1915605
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17470165
Samples
Known GenesSERPINA13P
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5850065
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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