A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18263700



Internal ID20830740
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:125809120..125809875hg38UCSC Ensembl
chr4:126730275..126731030hg19UCSC Ensembl
Cytoband4q28.1
Allele length
AssemblyAllele length
hg38756
hg19756
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6566350
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18263700
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00014


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