A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5849641



Internal ID22624576
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:64096798..64100950hg38UCSC Ensembl
chrUn_gl000211:128351..132503hg19UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg384153
hg194153
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17513960, nssv17513959
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5849641
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