A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17382407



Internal ID22440277
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:2723141..2733978hg38UCSC Ensembl
chr16:2773142..2783979hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3810838
hg1910838
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5945783
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17382407
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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