A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18268574



Internal ID20835614
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:116273816..116274456hg38UCSC Ensembl
chr6:116594979..116595619hg19UCSC Ensembl
Cytoband6q22.1
Allele length
AssemblyAllele length
hg38641
hg19641
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6568185
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18268574
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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