A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18258385



Internal ID20825426
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:75698970..75699719hg38UCSC Ensembl
chr2:75926096..75926845hg19UCSC Ensembl
Cytoband2p12
Allele length
AssemblyAllele length
hg38750
hg19750
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6548282
Supporting Variants
Samples
Known GenesGCFC2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18258385
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00014


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer