A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17399106



Internal ID22456976
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:44674945..44675249hg38UCSC Ensembl
chr22:45070825..45071129hg19UCSC Ensembl
Cytoband22q13.31
Allele length
AssemblyAllele length
hg38305
hg19305
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5965525
Supporting Variants
Samples
Known GenesPRR5
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17399106
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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