A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6104574



Internal ID22013807
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:27019694..27019694hg38UCSC Ensembl
chr22:27415657..27415657hg19UCSC Ensembl
Cytoband22q12.1
Allele length
AssemblyAllele length
hg3861
hg1961
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17644664
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6104574
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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