A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17376502



Internal ID22602171
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:68583438..68589504hg38UCSC Ensembl
chr16:68617341..68623407hg19UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg386067
hg196067
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5940720
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17376502
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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