A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4755725



Internal ID20531585
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:49926555..49926555hg38UCSC Ensembl
chr22:50320203..50320203hg19UCSC Ensembl
Cytoband22q13.33
Allele length
AssemblyAllele length
hg38154
hg19154
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16270705
Samples
Known GenesCRELD2
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4755725
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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