A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18248745



Internal ID20815785
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:174710924..174711526hg38UCSC Ensembl
chr1:174680062..174680664hg19UCSC Ensembl
Cytoband1q25.1
Allele length
AssemblyAllele length
hg38603
hg19603
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6538837
Supporting Variants
Samples
Known GenesRABGAP1L
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18248745
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