A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17467977



Internal ID22525866
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:108238476..108250743hg38UCSC Ensembl
chr13:108890824..108903091hg19UCSC Ensembl
Cytoband13q33.3
Allele length
AssemblyAllele length
hg3812268
hg1912268
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5864668
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17467977
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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