A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5830821



Internal ID22605756
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:95766855..95769104hg38UCSC Ensembl
chr1:96232411..96234660hg19UCSC Ensembl
Cytoband1p21.3
Allele length
AssemblyAllele length
hg382250
hg192250
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17482504
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5830821
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