A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18022907



Internal ID20589947
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:93907811..93909155hg38UCSC Ensembl
chr14:94374157..94375501hg19UCSC Ensembl
Cytoband14q32.12
Allele length
AssemblyAllele length
hg381345
hg191345
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6496125
Supporting Variants
Samples
Known GenesFAM181A-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18022907
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00031


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