A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16288958



Internal ID20498176
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:43343644..43343644hg38UCSC Ensembl
chr4:43345661..43345661hg19UCSC Ensembl
Cytoband4p13
Allele length
AssemblyAllele length
hg38123
hg19123
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4755351
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16288958
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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