A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6023199



Internal ID21932542
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:30788976..30789129hg38UCSC Ensembl
chr18:28368942..28369095hg19UCSC Ensembl
Cytoband18q12.1
Allele length
AssemblyAllele length
hg38154
hg19154
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17617909
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6023199
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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