A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16283078



Internal ID20492296
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:87533706..87533706hg38UCSC Ensembl
chr5:86829523..86829523hg19UCSC Ensembl
Cytoband5q14.3
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4758641
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16283078
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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