A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5906817



Internal ID22682020
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 StatusM
Merged Variants
Supporting Variantsnssv17427240
Samples
Known GenesTNFAIP8
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5906817
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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