A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6020934



Internal ID21930277
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:41430283..41432239hg38UCSC Ensembl
chr18:39010247..39012203hg19UCSC Ensembl
Cytoband18q12.3
Allele length
AssemblyAllele length
hg381957
hg191957
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17635676
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6020934
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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