A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5562349



Internal ID335307
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:24044690..24045305hg38UCSC Ensembl
chr6:24044918..24045533hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg38616
hg19616
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16980128
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5562349
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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