A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5849666



Internal ID22624601
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:109408454..109410980hg38UCSC Ensembl
chr12:109846259..109848785hg19UCSC Ensembl
Cytoband12q24.11
Allele length
AssemblyAllele length
hg382527
hg192527
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17455979
Samples
Known GenesMYO1H
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5849666
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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