A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18238070



Internal ID20805110
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:49468888..49474630hg38UCSC Ensembl
chr15:49761085..49766827hg19UCSC Ensembl
Cytoband15q21.2
Allele length
AssemblyAllele length
hg385743
hg195743
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6582207
Supporting Variants
Samples
Known GenesFAM227B, FGF7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18238070
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00018


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