A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18249220



Internal ID20816260
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:113721908..113722300hg38UCSC Ensembl
chr1:114264530..114264922hg19UCSC Ensembl
Cytoband1p13.2
Allele length
AssemblyAllele length
hg38393
hg19393
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6552715
Supporting Variants
Samples
Known GenesPHTF1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18249220
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