A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17487981



Internal ID22545898
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:15918724..15921714hg38UCSC Ensembl
chr21:17291044..17294034hg19UCSC Ensembl
Cytoband21q21.1
Allele length
AssemblyAllele length
hg382991
hg192991
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5869028
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17487981
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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