A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6552830



Internal ID20925957
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:143818027..143818754hg38UCSC Ensembl
chr2:144575596..144576323hg19UCSC Ensembl
Cytoband2q22.3
Allele length
AssemblyAllele length
hg38728
hg19728
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18254491
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6552830
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