A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6039189



Internal ID21948532
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:70211336..70211450hg38UCSC Ensembl
chr18:67878572..67878686hg19UCSC Ensembl
Cytoband18q22.2
Allele length
AssemblyAllele length
hg38115
hg19115
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17634899
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6039189
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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