A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5954012



Internal ID22729278
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:25811910..25864620hg38UCSC Ensembl
chr21:27184221..27236931hg19UCSC Ensembl
Cytoband21q21.3
Allele length
AssemblyAllele length
hg3852711
hg1952711
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1350n209
Supporting Variantsnssv17408696
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5954012
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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