A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17629287



Internal ID21821334
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:6430823..6430823hg38UCSC Ensembl
chr18:6430822..6430822hg19UCSC Ensembl
Cytoband18p11.31
Allele length
AssemblyAllele length
hg38251
hg19251
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6103796
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17629287
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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