A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16275682



Internal ID20484900
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:91557163..91557342hg38UCSC Ensembl
chr14:92023507..92023686hg19UCSC Ensembl
Cytoband14q32.12
Allele length
AssemblyAllele length
hg38180
hg19180
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4735829
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16275682
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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