A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16291813



Internal ID20501031
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:76984481..76984534hg38UCSC Ensembl
chr5:76280306..76280359hg19UCSC Ensembl
Cytoband5q13.3
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4745076
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16291813
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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