A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16293576



Internal ID20502794
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:178232830..178232830hg38UCSC Ensembl
chr5:177659831..177659831hg19UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg3893
hg1993
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4756096
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16293576
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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