A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6565964



Internal ID20939035
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:77257732..78114933hg38UCSC Ensembl
chr4:78178885..79036087hg19UCSC Ensembl
Cytoband4q21.1
Allele length
AssemblyAllele length
hg38857202
hg19857203
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18265307
Samples
Known GenesCNOT6L, CXCL13, FRAS1, MRPL1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6565964
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