A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17733657



Internal ID157323
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:63359372..63462814hg38UCSC Ensembl
chr20:61990724..62094167hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg38103443
hg19103444
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6146774
Supporting Variants
Samples
Known GenesCHRNA4, KCNQ2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17733657
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000312


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