A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5563089



Internal ID336026
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:24663738..24664151hg38UCSC Ensembl
chr1:24990229..24990642hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg38414
hg19414
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16902375
Samples
Known GenesSRRM1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5563089
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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