A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6076891



Internal ID21986124
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:121961158..121961158hg38UCSC Ensembl
chr6:122282304..122282304hg19UCSC Ensembl
Cytoband6q22.31
Allele length
AssemblyAllele length
hg38250
hg19250
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17560871
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6076891
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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