A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16268296



Internal ID20477514
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:11637902..11637970hg38UCSC Ensembl
chr16:11731758..11731826hg19UCSC Ensembl
Cytoband16p13.13
Allele length
AssemblyAllele length
hg3869
hg1969
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4734560
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16268296
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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