A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16281084



Internal ID20490302
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:26727079..26727079hg38UCSC Ensembl
chr18:24307043..24307043hg19UCSC Ensembl
Cytoband18q11.2
Allele length
AssemblyAllele length
hg38203
hg19203
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4759669
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16281084
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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