A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17628714



Internal ID21820761
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:49953414..49953611hg38UCSC Ensembl
chr16:49987325..49987522hg19UCSC Ensembl
Cytoband16q12.1
Allele length
AssemblyAllele length
hg38198
hg19198
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6039673
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17628714
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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