A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16288086



Internal ID20497304
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:61968825..61969043hg38UCSC Ensembl
chr18:59636058..59636276hg19UCSC Ensembl
Cytoband18q21.33
Allele length
AssemblyAllele length
hg38219
hg19219
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4749020
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16288086
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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