A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6032212



Internal ID21941555
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:34790342..34790547hg38UCSC Ensembl
chr18:32370306..32370511hg19UCSC Ensembl
Cytoband18q12.1
Allele length
AssemblyAllele length
hg38206
hg19206
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17633305
Samples
Known GenesDTNA
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6032212
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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