A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6569480



Internal ID20942551
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:77814539..77815075hg38UCSC Ensembl
chr7:77443856..77444392hg19UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg38537
hg19537
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18276646
Samples
Known GenesPHTF2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6569480
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