A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17480332



Internal ID22538235
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:36041917..36044091hg38UCSC Ensembl
chr21:37414215..37416389hg19UCSC Ensembl
Cytoband21q22.12
Allele length
AssemblyAllele length
hg382175
hg192175
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5880807
Supporting Variants
Samples
Known GenesSETD4
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17480332
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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