A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17427240



Internal ID22485110
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:119356356..119367326hg38UCSC Ensembl
chr5:118692051..118703021hg19UCSC Ensembl
Cytoband5q23.1
Allele length
AssemblyAllele length
hg3810971
hg1910971
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5906817
Supporting Variants
Samples
Known GenesTNFAIP8
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17427240
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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