A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16269349



Internal ID20478567
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:27946543..27946604hg38UCSC Ensembl
chr16:27957864..27957925hg19UCSC Ensembl
Cytoband16p12.1
Allele length
AssemblyAllele length
hg3862
hg1962
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4730334
Supporting Variants
Samples
Known GenesGSG1L
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16269349
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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