A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5848882



Internal ID22623817
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:101303663..101306008hg38UCSC Ensembl
chr13:101956014..101958359hg19UCSC Ensembl
Cytoband13q33.1
Allele length
AssemblyAllele length
hg382346
hg192346
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17468669, nssv17468211
Samples
Known GenesNALCN
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5848882
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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