A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5563809



Internal ID336737
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:158810182..158810233hg38UCSC Ensembl
chr6:159231214..159231265hg19UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg381240
hg191240
Variant TypeCNV sva insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16989526
Samples
Known GenesEZR
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5563809
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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