A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17385641



Internal ID22443511
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:89884403..89897045hg38UCSC Ensembl
chr13:90536657..90549299hg19UCSC Ensembl
Cytoband13q31.3
Allele length
AssemblyAllele length
hg3812643
hg1912643
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5944598
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17385641
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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