A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18272052



Internal ID20839092
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:73622984..73624814hg38UCSC Ensembl
chr6:74332707..74334537hg19UCSC Ensembl
Cytoband6q13
Allele length
AssemblyAllele length
hg381831
hg191831
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6572224
Supporting Variants
Samples
Known GenesSLC17A5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18272052
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