A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17366837



Internal ID22592506
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:102507474..102509073hg38UCSC Ensembl
chr13:103159824..103161423hg19UCSC Ensembl
Cytoband13q33.1
Allele length
AssemblyAllele length
hg381600
hg191600
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5935601
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17366837
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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