A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5932392



Internal ID22707689
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:86323257..86324360hg38UCSC Ensembl
chr13:86975512..86976615hg19UCSC Ensembl
Cytoband13q31.1
Allele length
AssemblyAllele length
hg381104
hg191104
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17380249
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5932392
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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