A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16276277



Internal ID20485495
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:36414978..36427193hg38UCSC Ensembl
chr20:35043381..35055596hg19UCSC Ensembl
Cytoband20q11.23
Allele length
AssemblyAllele length
hg3812216
hg1912216
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4748610
Supporting Variants
Samples
Known GenesDLGAP4
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16276277
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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