A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17469756



Internal ID22527646
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:91941091..91946295hg38UCSC Ensembl
chr14:92407435..92412639hg19UCSC Ensembl
Cytoband14q32.12
Allele length
AssemblyAllele length
hg385205
hg195205
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5856411
Supporting Variants
Samples
Known GenesFBLN5
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17469756
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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