A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5834309



Internal ID22609244
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:123729422..123739152hg38UCSC Ensembl
chr3:123448269..123457999hg19UCSC Ensembl
Cytoband3q21.1
Allele length
AssemblyAllele length
hg389731
hg199731
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1508n209
Supporting Variantsnssv17484387, nssv17484388
Samples
Known GenesMYLK
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5834309
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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