A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6569998



Internal ID20943069
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:49571429..49572070hg38UCSC Ensembl
chr6:49539142..49539783hg19UCSC Ensembl
Cytoband6p12.3
Allele length
AssemblyAllele length
hg38642
hg19642
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18272039
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6569998
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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