A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5558661



Internal ID331718
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:78301319..78885684hg38UCSC Ensembl
chr6:79011036..79595401hg19UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg38584366
hg19584366
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16987330
Samples
Known GenesIRAK1BP1
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5558661
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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