A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5938671



Internal ID22714054
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:22844980..22845476hg38UCSC Ensembl
chr16:22856301..22856797hg19UCSC Ensembl
Cytoband16p12.2
Allele length
AssemblyAllele length
hg38497
hg19497
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17373494
Samples
Known GenesHS3ST2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5938671
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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