A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6561555



Internal ID20934626
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:22637268..22964010hg38UCSC Ensembl
chr6:22637497..22964239hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg38326743
hg19326743
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18270832
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6561555
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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