A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5956865



Internal ID22732021
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:47732324..47732803hg38UCSC Ensembl
chr22:48128073..48128552hg19UCSC Ensembl
Cytoband22q13.31
Allele length
AssemblyAllele length
hg38480
hg19480
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17403907
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5956865
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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