A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5979694



Internal ID22754629
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:34436764..34436764hg38UCSC Ensembl
chr22:34832755..34832755hg19UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg38243
hg19243
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17402526
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5979694
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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