A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17451308



Internal ID22509180
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:103297795..103310709hg38UCSC Ensembl
chr13:103950145..103963059hg19UCSC Ensembl
Cytoband13q33.1
Allele length
AssemblyAllele length
hg3812915
hg1912915
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5853737
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17451308
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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