A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17483684



Internal ID22541591
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:107692444..107700768hg38UCSC Ensembl
chr3:107411291..107419615hg19UCSC Ensembl
Cytoband3q13.12
Allele length
AssemblyAllele length
hg388325
hg198325
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5834497
Supporting Variants
Samples
Known GenesBBX
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17483684
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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