A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6574935



Internal ID20948006
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:36868590..36869061hg38UCSC Ensembl
chr6:36836366..36836837hg19UCSC Ensembl
Cytoband6p21.2
Allele length
AssemblyAllele length
hg38472
hg19472
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18270726
Samples
Known GenesPPIL1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6574935
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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