A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6563956



Internal ID20937027
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:15895874..15898240hg38UCSC Ensembl
chr6:15896105..15898471hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg382367
hg192367
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6067n223
Supporting Variantsnssv18270484
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6563956
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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