A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4731635



Internal ID20507555
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 StatusM
Merged Variants
Supporting Variantsnssv16273586
Samples
Known GenesSGSM3
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4731635
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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