A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17378919



Internal ID22436789
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:22818656..22818809hg38UCSC Ensembl
chr16:22829977..22830130hg19UCSC Ensembl
Cytoband16p12.2
Allele length
AssemblyAllele length
hg38154
hg19154
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5929805
Supporting Variants
Samples
Known GenesHS3ST2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17378919
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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