A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6109601



Internal ID22018834
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:55081127..55081127hg38UCSC Ensembl
chr18:52748358..52748358hg19UCSC Ensembl
Cytoband18q21.2
Allele length
AssemblyAllele length
hg385956
hg195956
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17632359
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6109601
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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