A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6146977



Internal ID346183
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:64286625..64325812hg38UCSC Ensembl
chr20:62917978..62957165hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg3839188
hg1939188
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17733748
Samples
Known GenesLINC00266-1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6146977
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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