A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16287678



Internal ID20496896
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:77042422..77042476hg38UCSC Ensembl
chr5:76338247..76338301hg19UCSC Ensembl
Cytoband5q13.3
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4750006
Supporting Variants
Samples
Known GenesAGGF1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16287678
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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