A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17620537



Internal ID21812584
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:27827886..27827944hg38UCSC Ensembl
chr16:27839207..27839265hg19UCSC Ensembl
Cytoband16p12.1
Allele length
AssemblyAllele length
hg3859
hg1959
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6034044
Supporting Variants
Samples
Known GenesGSG1L
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17620537
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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