A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16273586



Internal ID20482804
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:40398214..40399235hg38UCSC Ensembl
chr22:40794218..40795239hg19UCSC Ensembl
Cytoband22q13.1
Allele length
AssemblyAllele length
hg381022
hg191022
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4731635
Supporting Variants
Samples
Known GenesSGSM3
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16273586
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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