A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5952997



Internal ID22728293
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:36803513..36803575hg38UCSC Ensembl
chr22:37199557..37199619hg19UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg3863
hg1963
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17392108
Samples
Known GenesPVALB
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5952997
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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