A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17459834



Internal ID22517720
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:111936523..111943176hg38UCSC Ensembl
chr13:112590837..112597490hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg386654
hg196654
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5856929
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17459834
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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