A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17379667



Internal ID22437537
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:86605554..86628127hg38UCSC Ensembl
chr16:86639160..86661733hg19UCSC Ensembl
Cytoband16q24.1
Allele length
AssemblyAllele length
hg3822574
hg1922574
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5940086
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17379667
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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