A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17409144



Internal ID22467014
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:29761310..29763330hg38UCSC Ensembl
chr22:30157299..30159319hg19UCSC Ensembl
Cytoband22q12.2
Allele length
AssemblyAllele length
hg382021
hg192021
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5967392
Supporting Variants
Samples
Known GenesZMAT5
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17409144
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.002


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