A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17385065



Internal ID22442935
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:64243097..64339712hg38UCSC Ensembl
chr16:64277001..64373616hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg3896616
hg1996616
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5939985
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17385065
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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