A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18019725



Internal ID20586765
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:50157501..50158600hg38UCSC Ensembl
chr14:50624219..50625318hg19UCSC Ensembl
Cytoband14q21.3
Allele length
AssemblyAllele length
hg381100
hg191100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6487980
Supporting Variants
Samples
Known GenesSOS2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18019725
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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