A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18272216



Internal ID20839256
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:104924050..104924506hg38UCSC Ensembl
chr7:104564497..104564953hg19UCSC Ensembl
Cytoband7q22.3
Allele length
AssemblyAllele length
hg38457
hg19457
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6556347
Supporting Variants
Samples
Known GenesLHFPL3-AS2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18272216
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