A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6030829



Internal ID21940172
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:76065124..76074441hg38UCSC Ensembl
chr18:73777079..73786396hg19UCSC Ensembl
Cytoband18q23
Allele length
AssemblyAllele length
hg389318
hg199318
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17637498
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6030829
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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