A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5830310



Internal ID22605245
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:39065271..39073782hg38UCSC Ensembl
chr1:39530943..39539454hg19UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg388512
hg198512
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17451268
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5830310
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