A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18257342



Internal ID20824382
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:232051611..232052320hg38UCSC Ensembl
chr2:232916321..232917030hg19UCSC Ensembl
Cytoband2q37.1
Allele length
AssemblyAllele length
hg38710
hg19710
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6551612
Supporting Variants
Samples
Known GenesDIS3L2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18257342
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