A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6573189



Internal ID20946260
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:122663315..122669464hg38UCSC Ensembl
chr6:122984460..122990609hg19UCSC Ensembl
Cytoband6q22.31
Allele length
AssemblyAllele length
hg386150
hg196150
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18271127
Samples
Known GenesPKIB
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6573189
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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