A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17380788



Internal ID22438658
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:56620919..56621884hg38UCSC Ensembl
chr16:56654831..56655796hg19UCSC Ensembl
Cytoband16q12.2
Allele length
AssemblyAllele length
hg38966
hg19966
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5933392
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17380788
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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