A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17373985



Internal ID22599654
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:75136880..75148150hg38UCSC Ensembl
chr16:75170778..75182048hg19UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg3811271
hg1911271
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5945404
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17373985
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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