A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17381899



Internal ID22439769
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:13263465..13273533hg38UCSC Ensembl
chr16:13357322..13367390hg19UCSC Ensembl
Cytoband16p13.12
Allele length
AssemblyAllele length
hg3810069
hg1910069
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5928696
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17381899
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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