A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5963950



Internal ID22738885
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:14383364..14393378hg38UCSC Ensembl
chr21:15755685..15765699hg19UCSC Ensembl
Cytoband21q11.2
Allele length
AssemblyAllele length
hg3810015
hg1910015
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17405413
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5963950
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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