A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6549080



Internal ID20922251
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:175818480..175819882hg38UCSC Ensembl
chr2:176683208..176684610hg19UCSC Ensembl
Cytoband2q31.1
Allele length
AssemblyAllele length
hg381403
hg191403
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18256174
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6549080
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