A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6554572



Internal ID20927665
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:176606158..176614367hg38UCSC Ensembl
chr2:177470886..177479095hg19UCSC Ensembl
Cytoband2q31.1
Allele length
AssemblyAllele length
hg388210
hg198210
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18256194
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6554572
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