A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6105518



Internal ID22014751
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:57328073..57328073hg38UCSC Ensembl
chr18:54995304..54995304hg19UCSC Ensembl
Cytoband18q21.31
Allele length
AssemblyAllele length
hg38285
hg19285
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17625181
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6105518
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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