A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5860964



Internal ID22635899
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:29173811..29175041hg38UCSC Ensembl
chr13:29747948..29749178hg19UCSC Ensembl
Cytoband13q12.3
Allele length
AssemblyAllele length
hg381231
hg191231
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17458860
Samples
Known GenesMTUS2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5860964
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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