A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6561481



Internal ID20934552
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:25156420..25157612hg38UCSC Ensembl
chr4:25158042..25159234hg19UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg381193
hg191193
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18265622
Samples
Known GenesSEPSECS
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6561481
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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