A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17417710



Internal ID22475580
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:137871408..137873734hg38UCSC Ensembl
chr6:138192545..138194871hg19UCSC Ensembl
Cytoband6q23.3
Allele length
AssemblyAllele length
hg382327
hg192327
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5901279
Supporting Variants
Samples
Known GenesTNFAIP3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17417710
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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