A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5862568



Internal ID22637503
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:97289311..97291765hg38UCSC Ensembl
chr13:97941565..97944019hg19UCSC Ensembl
Cytoband13q32.1
Allele length
AssemblyAllele length
hg382455
hg192455
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17462655
Samples
Known GenesMBNL2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5862568
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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