A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5842395



Internal ID22617330
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:32259974..32261173hg38UCSC Ensembl
chr5:32260080..32261279hg19UCSC Ensembl
Cytoband5p13.3
Allele length
AssemblyAllele length
hg381200
hg191200
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17496591
Samples
Known GenesMTMR12
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5842395
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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