A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16259648



Internal ID20468866
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:38183446..38183575hg38UCSC Ensembl
chr18:35763410..35763539hg19UCSC Ensembl
Cytoband18q12.2
Allele length
AssemblyAllele length
hg38130
hg19130
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4748121
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16259648
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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