A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5953952



Internal ID22729220
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:47260818..47260889hg38UCSC Ensembl
chr22:47656568..47656639hg19UCSC Ensembl
Cytoband22q13.31
Allele length
AssemblyAllele length
hg3872
hg1972
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17396217
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5953952
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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