A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5562588



Internal ID335537
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:106550641..106550667hg38UCSC Ensembl
chr6:106998516..106998542hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg3827
hg1927
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16986294
Samples
Known GenesAIM1
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5562588
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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