A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17468272



Internal ID22526161
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:65415414..65416413hg38UCSC Ensembl
chr14:65882132..65883131hg19UCSC Ensembl
Cytoband14q23.3
Allele length
AssemblyAllele length
hg381000
hg191000
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5855817
Supporting Variants
Samples
Known GenesFUT8
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17468272
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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