A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18263447



Internal ID20830487
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:106289546..106290207hg38UCSC Ensembl
chr4:107210703..107211364hg19UCSC Ensembl
Cytoband4q24
Allele length
AssemblyAllele length
hg38662
hg19662
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6568662
Supporting Variants
Samples
Known GenesTBCK
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18263447
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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