A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6146861



Internal ID346067
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:45886625..45896625hg38UCSC Ensembl
chr20:44515264..44525264hg19UCSC Ensembl
Cytoband20q13.12
Allele length
AssemblyAllele length
hg3810001
hg1910001
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17732644
Samples
Known GenesCTSA, NEURL2, SPATA25
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6146861
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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