A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5864862



Internal ID22639797
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:29147970..29195716hg38UCSC Ensembl
chr13:29722107..29769853hg19UCSC Ensembl
Cytoband13q12.3
Allele length
AssemblyAllele length
hg3847747
hg1947747
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17463659
Samples
Known GenesMTUS2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5864862
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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