A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17520955



Internal ID21845314
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:78449483..78449483hg38UCSC Ensembl
chr1:78915168..78915168hg19UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg38311
hg19311
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6055162
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17520955
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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