A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17390047



Internal ID22447917
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:17900617..17902558hg38UCSC Ensembl
chr21:19272934..19274875hg19UCSC Ensembl
Cytoband21q21.1
Allele length
AssemblyAllele length
hg381942
hg191942
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5959320
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17390047
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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