A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16285517



Internal ID20494735
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:144413109..144413171hg38UCSC Ensembl
chr8:145638493..145638555hg19UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg3863
hg1963
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4741027
Supporting Variants
Samples
Known GenesSLC39A4
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16285517
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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