A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6068004



Internal ID21977237
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:28113940..28113940hg38UCSC Ensembl
chr6:28081718..28081718hg19UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17573267
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6068004
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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