A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6021975



Internal ID21931318
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:57327638..57327941hg38UCSC Ensembl
chr18:54994869..54995172hg19UCSC Ensembl
Cytoband18q21.31
Allele length
AssemblyAllele length
hg38304
hg19304
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17618297
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6021975
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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