A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5866864



Internal ID22641799
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:101386921..101392287hg38UCSC Ensembl
chr13:102039272..102044638hg19UCSC Ensembl
Cytoband13q33.1
Allele length
AssemblyAllele length
hg385367
hg195367
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17463082
Samples
Known GenesNALCN
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5866864
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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