A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18022909



Internal ID20589949
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:93994889..94003407hg38UCSC Ensembl
chr14:94461235..94469753hg19UCSC Ensembl
Cytoband14q32.12
Allele length
AssemblyAllele length
hg388519
hg198519
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6496241
Supporting Variants
Samples
Known GenesLINC00521
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18022909
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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