A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17523729



Internal ID21848088
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:223206322..223206322hg38UCSC Ensembl
chr2:224071040..224071040hg19UCSC Ensembl
Cytoband2q36.1
Allele length
AssemblyAllele length
hg38112
hg19112
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6042481
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17523729
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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