A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5834872



Internal ID22609807
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:123714621..123736015hg38UCSC Ensembl
chr3:123433468..123454862hg19UCSC Ensembl
Cytoband3q21.1
Allele length
AssemblyAllele length
hg3821395
hg1921395
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17484386
Samples
Known GenesMYLK
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5834872
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