A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18268517



Internal ID20835557
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:112587707..112590049hg38UCSC Ensembl
chr6:112908909..112911251hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg382343
hg192343
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6568032
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18268517
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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