A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6568693



Internal ID20941764
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:99068801..99069209hg38UCSC Ensembl
chr4:99989952..99990360hg19UCSC Ensembl
Cytoband4q23
Allele length
AssemblyAllele length
hg38409
hg19409
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18266119
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6568693
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