A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6025983



Internal ID21935326
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:30862927..30870956hg38UCSC Ensembl
chr18:28442893..28450922hg19UCSC Ensembl
Cytoband18q12.1
Allele length
AssemblyAllele length
hg388030
hg198030
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17636403
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6025983
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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