A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5829933



Internal ID22604868
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:26651235..26661063hg38UCSC Ensembl
chr1:26977726..26987554hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg389829
hg199829
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17463672
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5829933
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