A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6111091



Internal ID22020324
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:46201420..46201420hg38UCSC Ensembl
chr21:47621334..47621334hg19UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg38174
hg19174
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17638671
Samples
Known GenesLSS
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6111091
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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