A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16278657



Internal ID20487875
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:94501976..94502236hg38UCSC Ensembl
chr13:95154230..95154490hg19UCSC Ensembl
Cytoband13q32.1
Allele length
AssemblyAllele length
hg38261
hg19261
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4736217
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16278657
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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