A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5960990



Internal ID22735949
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:38340473..38340686hg38UCSC Ensembl
chr21:39712395..39712608hg19UCSC Ensembl
Cytoband21q22.2
Allele length
AssemblyAllele length
hg38214
hg19214
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17409179
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5960990
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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