A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17378420



Internal ID22436290
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:33799438..33801219hg38UCSC Ensembl
chr13:34373575..34375356hg19UCSC Ensembl
Cytoband13q13.2
Allele length
AssemblyAllele length
hg381782
hg191782
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5944032
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17378420
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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