A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6030451



Internal ID21939794
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:37934440..37934499hg38UCSC Ensembl
chr18:35514404..35514463hg19UCSC Ensembl
Cytoband18q12.2
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17633877
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6030451
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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