A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18250035



Internal ID20817075
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:20817830..20818506hg38UCSC Ensembl
chr1:21144323..21144999hg19UCSC Ensembl
Cytoband1p36.12
Allele length
AssemblyAllele length
hg38677
hg19677
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6542068
Supporting Variants
Samples
Known GenesEIF4G3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18250035
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00017


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