A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16269651



Internal ID20478869
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:19349380..19349457hg38UCSC Ensembl
chr16:19360702..19360779hg19UCSC Ensembl
Cytoband16p12.3
Allele length
AssemblyAllele length
hg3878
hg1978
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4734254
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16269651
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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