A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18258532



Internal ID20825572
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:206666248..206666966hg38UCSC Ensembl
chr2:207530972..207531690hg19UCSC Ensembl
Cytoband2q33.3
Allele length
AssemblyAllele length
hg38719
hg19719
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6540209
Supporting Variants
Samples
Known GenesDYTN
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18258532
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer