A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17465588



Internal ID22523477
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:73616559..73619079hg38UCSC Ensembl
chr14:74083263..74085783hg19UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg382521
hg192521
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5862449
Supporting Variants
Samples
Known GenesACOT6
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17465588
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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