A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16278074



Internal ID20487292
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:166073853..166074531hg38UCSC Ensembl
chr5:165500858..165501536hg19UCSC Ensembl
Cytoband5q34
Allele length
AssemblyAllele length
hg38679
hg19679
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4736631
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16278074
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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