A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6547569



Internal ID20920770
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:27331488..27331939hg38UCSC Ensembl
chr2:27554355..27554806hg19UCSC Ensembl
Cytoband2p23.3
Allele length
AssemblyAllele length
hg38452
hg19452
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18257546
Samples
Known GenesGTF3C2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6547569
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