A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5564063



Internal ID336985
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:146863181..146927794hg38UCSC Ensembl
chr6:147184317..147248930hg19UCSC Ensembl
Cytoband6q24.3
Allele length
AssemblyAllele length
hg3864614
hg1964614
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16989870
Samples
Known GenesSTXBP5-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5564063
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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