A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18261420



Internal ID20828460
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:52963724..52964238hg38UCSC Ensembl
chr3:52997740..52998254hg19UCSC Ensembl
Cytoband3p21.1
Allele length
AssemblyAllele length
hg38515
hg19515
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6544497
Supporting Variants
Samples
Known GenesSFMBT1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18261420
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