A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17397785



Internal ID22455655
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:36040731..36040781hg38UCSC Ensembl
chr22:36436779..36436829hg19UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg3851
hg1951
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5954930
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17397785
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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