A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17622675



Internal ID21814722
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:50609984..50609984hg38UCSC Ensembl
chr20:49226521..49226521hg19UCSC Ensembl
Cytoband20q13.13
Allele length
AssemblyAllele length
hg3858
hg1958
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6111310
Supporting Variants
Samples
Known GenesFAM65C
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17622675
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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