A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17634186



Internal ID21826233
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:35153557..35156626hg38UCSC Ensembl
chr18:32733521..32736590hg19UCSC Ensembl
Cytoband18q12.2
Allele length
AssemblyAllele length
hg383070
hg193070
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6036803
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17634186
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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