A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6566123



Internal ID20939194
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:2552104..2553371hg38UCSC Ensembl
chr6:2552338..2553605hg19UCSC Ensembl
Cytoband6p25.2
Allele length
AssemblyAllele length
hg381268
hg191268
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18270901
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6566123
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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