A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18263634



Internal ID20830674
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:121192440..121193042hg38UCSC Ensembl
chr4:122113595..122114197hg19UCSC Ensembl
Cytoband4q27
Allele length
AssemblyAllele length
hg38603
hg19603
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6559544
Supporting Variants
Samples
Known GenesTNIP3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18263634
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer