A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6546522



Internal ID20919738
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:196124616..196125279hg38UCSC Ensembl
chr2:196989340..196990003hg19UCSC Ensembl
Cytoband2q32.3
Allele length
AssemblyAllele length
hg38664
hg19664
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18256006
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6546522
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