A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5930877



Internal ID22706151
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:87291687..87311567hg38UCSC Ensembl
chr13:87943942..87963822hg19UCSC Ensembl
Cytoband13q31.2
Allele length
AssemblyAllele length
hg3819881
hg1919881
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17373057
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5930877
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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