A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5866581



Internal ID22641516
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:94644106..94648430hg38UCSC Ensembl
chr14:95110443..95114767hg19UCSC Ensembl
Cytoband14q32.13
Allele length
AssemblyAllele length
hg384325
hg194325
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17470166
Samples
Known GenesSERPINA13P
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5866581
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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