A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5851967



Internal ID22626902
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:32479640..32487049hg38UCSC Ensembl
chr13:33053777..33061186hg19UCSC Ensembl
Cytoband13q13.1
Allele length
AssemblyAllele length
hg387410
hg197410
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17455015
Samples
Known GenesN4BP2L2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5851967
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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