A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18271653



Internal ID20838693
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:77820354..77821747hg38UCSC Ensembl
chr6:78530071..78531464hg19UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg381394
hg191394
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6566498
Supporting Variants
Samples
Known GenesMEI4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18271653
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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