A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17397129



Internal ID22454999
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:27088316..27094890hg38UCSC Ensembl
chr21:28460635..28467209hg19UCSC Ensembl
Cytoband21q21.3
Allele length
AssemblyAllele length
hg386575
hg196575
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5953926
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17397129
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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