A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17533264



Internal ID21857620
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:144361749..144361749hg38UCSC Ensembl
chr2:145119316..145119316hg19UCSC Ensembl
Cytoband2q22.3
Allele length
AssemblyAllele length
hg38388
hg19388
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6060423
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17533264
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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