A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18274408



Internal ID20841448
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:139173245..139175007hg38UCSC Ensembl
chr7:138857991..138859753hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg381763
hg191763
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6565841
Supporting Variants
Samples
Known GenesTTC26
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18274408
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