A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6574821



Internal ID20947892
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:106676033..106676943hg38UCSC Ensembl
chr6:107123908..107124818hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg38911
hg19911
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18269769
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6574821
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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