A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17488442



Internal ID22546359
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:24178820..24202152hg38UCSC Ensembl
chr21:25551133..25574465hg19UCSC Ensembl
Cytoband21q21.2
Allele length
AssemblyAllele length
hg3823333
hg1923333
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5879801
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17488442
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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