A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17541897



Internal ID21866252
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:42021918..42022102hg38UCSC Ensembl
chr4:42023935..42024119hg19UCSC Ensembl
Cytoband4p13
Allele length
AssemblyAllele length
hg38185
hg19185
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5997310
Supporting Variants
Samples
Known GenesSLC30A9
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17541897
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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