A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17493769



Internal ID22551699
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:119356299..119357398hg38UCSC Ensembl
chr5:118691994..118693093hg19UCSC Ensembl
Cytoband5q23.1
Allele length
AssemblyAllele length
hg381100
hg191100
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5840723
Supporting Variants
Samples
Known GenesTNFAIP8
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17493769
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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