A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6561677



Internal ID20934748
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:102886215..102886772hg38UCSC Ensembl
chr4:103807372..103807929hg19UCSC Ensembl
Cytoband4q24
Allele length
AssemblyAllele length
hg38558
hg19558
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18263395
Samples
Known GenesCISD2, SLC9B1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6561677
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