A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5560105



Internal ID333119
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:6957459..7126409hg38UCSC Ensembl
chr6:6957692..7126642hg19UCSC Ensembl
Cytoband6p24.3
Allele length
AssemblyAllele length
hg38168951
hg19168951
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16978090
Samples
Known GenesRREB1
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5560105
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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