A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6552657



Internal ID20925783
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:135034937..135036058hg38UCSC Ensembl
chr2:135792507..135793628hg19UCSC Ensembl
Cytoband2q21.3
Allele length
AssemblyAllele length
hg381122
hg191122
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18255280
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6552657
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