A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17493771



Internal ID22551701
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:119379321..119382940hg38UCSC Ensembl
chr5:118715016..118718635hg19UCSC Ensembl
Cytoband5q23.1
Allele length
AssemblyAllele length
hg383620
hg193620
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5841019
Supporting Variants
Samples
Known GenesTNFAIP8
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17493771
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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