A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5426964



Internal ID205878
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:64287450..64334100hg38UCSC Ensembl
chr20:62918803..62965453hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg3846651
hg1946651
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17733750
Samples
Known GenesLINC00266-1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5426964
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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