A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5564017



Internal ID336941
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:73522706..73524776hg38UCSC Ensembl
chr6:74232429..74234499hg19UCSC Ensembl
Cytoband6q13
Allele length
AssemblyAllele length
hg382071
hg192071
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16984168
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5564017
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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