A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5554806



Internal ID327979
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:23404085..23599492hg38UCSC Ensembl
chr9:23404083..23599490hg19UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg38195408
hg19195408
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17021940
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5554806
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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