A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17453187



Internal ID22511061
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:103282054..103303047hg38UCSC Ensembl
chr13:103934404..103955397hg19UCSC Ensembl
Cytoband13q33.1
Allele length
AssemblyAllele length
hg3820994
hg1920994
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5857232
Supporting Variants
Samples
Known GenesMIR548AS
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17453187
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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