A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5829476



Internal ID22604411
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:230481159..230489682hg38UCSC Ensembl
chr1:230616905..230625428hg19UCSC Ensembl
Cytoband1q42.13
Allele length
AssemblyAllele length
hg388524
hg198524
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17458933
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5829476
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