A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4731508



Internal ID20507428
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:31114963..31115017hg38UCSC Ensembl
chr22:31510949..31511003hg19UCSC Ensembl
Cytoband22q12.2
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16268364
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4731508
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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