A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18251914



Internal ID20818954
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:86969937..86970683hg38UCSC Ensembl
chr1:87435620..87436366hg19UCSC Ensembl
Cytoband1p22.3
Allele length
AssemblyAllele length
hg38747
hg19747
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6548304
Supporting Variants
Samples
Known GenesHS2ST1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18251914
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