A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18261488



Internal ID20828528
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:56631602..56632342hg38UCSC Ensembl
chr3:56665630..56666370hg19UCSC Ensembl
Cytoband3p14.3
Allele length
AssemblyAllele length
hg38741
hg19741
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6536814
Supporting Variants
Samples
Known GenesFAM208A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18261488
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