A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17459295



Internal ID22517178
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:151358773..151366909hg38UCSC Ensembl
chr1:151331249..151339385hg19UCSC Ensembl
Cytoband1q21.3
Allele length
AssemblyAllele length
hg388137
hg198137
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5828135
Supporting Variants
Samples
Known GenesSELENBP1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17459295
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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