A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17488370



Internal ID22546287
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:18568278..18569640hg38UCSC Ensembl
chr21:19940596..19941958hg19UCSC Ensembl
Cytoband21q21.1
Allele length
AssemblyAllele length
hg381363
hg191363
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5870400
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17488370
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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