A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16274853



Internal ID20484071
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:50632085..50632810hg38UCSC Ensembl
chr20:49248622..49249347hg19UCSC Ensembl
Cytoband20q13.13
Allele length
AssemblyAllele length
hg38726
hg19726
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4738006
Supporting Variants
Samples
Known GenesFAM65C
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16274853
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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