A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18269236



Internal ID20836276
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:120593241..123536832hg38UCSC Ensembl
chr6:120914387..123857977hg19UCSC Ensembl
Cytoband6q22.31
Allele length
AssemblyAllele length
hg382943592
hg192943591
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6568941
Supporting Variants
Samples
Known GenesCLVS2, FABP7, GJA1, HSF2, PKIB, SERINC1, SMPDL3A, TBC1D32, TRDN
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18269236
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