A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17635417



Internal ID21827464
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:50617059..50618181hg38UCSC Ensembl
chr20:49233596..49234718hg19UCSC Ensembl
Cytoband20q13.13
Allele length
AssemblyAllele length
hg381123
hg191123
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6041870
Supporting Variants
Samples
Known GenesFAM65C
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17635417
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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