A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5563569



Internal ID336501
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:76686228..76794990hg38UCSC Ensembl
chr17:74682310..74791072hg19UCSC Ensembl
Cytoband17q25.1
Allele length
AssemblyAllele length
hg38108763
hg19108763
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17714744
Samples
Known GenesJMJD6, METTL23, MFSD11, MIR636, MXRA7, SRSF2
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5563569
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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