A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17479333



Internal ID22537235
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:5830798..5840842hg38UCSC Ensembl
chr19:5830809..5840853hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg3810045
hg1910045
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5868320
Supporting Variants
Samples
Known GenesFUT6
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17479333
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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