A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5955689



Internal ID22730888
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:44749943..44750222hg38UCSC Ensembl
chr21:46169858..46170137hg19UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg38280
hg19280
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17403697
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5955689
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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