A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18271488



Internal ID20838528
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:52267528..52270025hg38UCSC Ensembl
chr6:52132326..52134823hg19UCSC Ensembl
Cytoband6p12.2
Allele length
AssemblyAllele length
hg382498
hg192498
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6565647
Supporting Variants
Samples
Known GenesMCM3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18271488
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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