A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18271798



Internal ID20838838
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:127724468..127734962hg38UCSC Ensembl
chr6:128045613..128056107hg19UCSC Ensembl
Cytoband6q22.33
Allele length
AssemblyAllele length
hg3810495
hg1910495
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6575124
Supporting Variants
Samples
Known GenesTHEMIS
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18271798
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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