A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17630259



Internal ID21822306
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:12169585..12175890hg38UCSC Ensembl
chr18:12169584..12175889hg19UCSC Ensembl
Cytoband18p11.21
Allele length
AssemblyAllele length
hg386306
hg196306
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6030092
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17630259
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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