A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16279831



Internal ID20489049
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:76336020..76336076hg38UCSC Ensembl
chr5:75631845..75631901hg19UCSC Ensembl
Cytoband5q13.3
Allele length
AssemblyAllele length
hg3857
hg1957
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4745388
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16279831
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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