A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6567552



Internal ID20940623
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:151459127..151460105hg38UCSC Ensembl
chr6:151780262..151781240hg19UCSC Ensembl
Cytoband6q25.1
Allele length
AssemblyAllele length
hg38979
hg19979
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18269388
Samples
Known GenesC6orf211
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6567552
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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