A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17371355



Internal ID22597024
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:31693936..31698972hg38UCSC Ensembl
chr14:32163142..32168178hg19UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg385037
hg195037
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5942422
Supporting Variants
Samples
Known GenesNUBPL
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17371355
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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