A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18271296



Internal ID20838336
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:42461726..42462563hg38UCSC Ensembl
chr6:42429464..42430301hg19UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg38838
hg19838
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6564014
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18271296
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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