A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17488498



Internal ID22546415
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:33160309..33189788hg38UCSC Ensembl
chr21:34532615..34562093hg19UCSC Ensembl
Cytoband21q22.11
Allele length
AssemblyAllele length
hg3829480
hg1929479
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5881473
Supporting Variants
Samples
Known GenesC21orf54
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17488498
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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