A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16292798



Internal ID20502016
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:65886078..65886078hg38UCSC Ensembl
chr5:65181906..65181906hg19UCSC Ensembl
Cytoband5q12.3
Allele length
AssemblyAllele length
hg3884
hg1984
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4750572
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16292798
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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