A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18248077



Internal ID20815117
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:17041526..17043095hg38UCSC Ensembl
chr1:17368021..17369590hg19UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg381570
hg191570
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6552449
Supporting Variants
Samples
Known GenesSDHB
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18248077
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