A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16283280



Internal ID20492498
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:18257449..18257449hg38UCSC Ensembl
chr5:18257558..18257558hg19UCSC Ensembl
Cytoband5p15.1
Allele length
AssemblyAllele length
hg38301
hg19301
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4757506
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16283280
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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