A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17383374



Internal ID22441244
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:57855887..57858859hg38UCSC Ensembl
chr14:58322605..58325577hg19UCSC Ensembl
Cytoband14q23.1
Allele length
AssemblyAllele length
hg382973
hg192973
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5943872
Supporting Variants
Samples
Known GenesSLC35F4
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17383374
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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