A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5828982



Internal ID22603917
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:19740725..19744749hg38UCSC Ensembl
chr1:20067218..20071242hg19UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg384025
hg194025
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17451440
Samples
Known GenesTMCO4
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5828982
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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