A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18252018



Internal ID20819058
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:91229487..91230299hg38UCSC Ensembl
chr1:91695044..91695856hg19UCSC Ensembl
Cytoband1p22.2
Allele length
AssemblyAllele length
hg38813
hg19813
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6541885
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18252018
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