A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18269837



Internal ID20836877
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:108182269..108182977hg38UCSC Ensembl
chr6:108503473..108504181hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg38709
hg19709
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6574155
Supporting Variants
Samples
Known GenesNR2E1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18269837
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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