A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16276578



Internal ID20485796
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:25033498..25033498hg38UCSC Ensembl
chr18:22613462..22613462hg19UCSC Ensembl
Cytoband18q11.2
Allele length
AssemblyAllele length
hg38449
hg19449
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4756264
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16276578
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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