A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5959703



Internal ID22734725
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:15514114..15514188hg38UCSC Ensembl
chr21:16886433..16886507hg19UCSC Ensembl
Cytoband21q21.1
Allele length
AssemblyAllele length
hg3875
hg1975
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17405537
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5959703
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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