A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5942655



Internal ID22718096
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:90696348..90696421hg38UCSC Ensembl
chr13:91348602..91348675hg19UCSC Ensembl
Cytoband13q31.3
Allele length
AssemblyAllele length
hg3874
hg1974
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17373392
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5942655
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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