A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5936886



Internal ID22712246
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:32564183..32564255hg38UCSC Ensembl
chr13:33138320..33138392hg19UCSC Ensembl
Cytoband13q13.1
Allele length
AssemblyAllele length
hg3873
hg1973
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17388648
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5936886
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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