A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17461627



Internal ID22519512
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:113934861..113936360hg38UCSC Ensembl
chr13:114637834..114639333hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg381500
hg191500
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5857253
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17461627
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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