A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17531815



Internal ID21856171
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:222472501..222472501hg38UCSC Ensembl
chr1:222645843..222645843hg19UCSC Ensembl
Cytoband1q41
Allele length
AssemblyAllele length
hg3857
hg1957
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6045536
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17531815
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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