A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5974525



Internal ID22749460
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:18829965..18829965hg38UCSC Ensembl
chr21:20202283..20202283hg19UCSC Ensembl
Cytoband21q21.1
Allele length
AssemblyAllele length
hg38177
hg19177
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17396143
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5974525
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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