A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18268518



Internal ID20835558
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:112629363..113770014hg38UCSC Ensembl
chr6:112950565..114091216hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg381140652
hg191140652
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6573256
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18268518
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.02185


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