A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6035475



Internal ID21944818
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:36276036..36276853hg38UCSC Ensembl
chr18:33855999..33856816hg19UCSC Ensembl
Cytoband18q12.2
Allele length
AssemblyAllele length
hg38818
hg19818
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17629652
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6035475
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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