A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6552735



Internal ID20925861
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:202996057..202996712hg38UCSC Ensembl
chr2:203860780..203861435hg19UCSC Ensembl
Cytoband2q33.2
Allele length
AssemblyAllele length
hg38656
hg19656
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18257786
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6552735
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