A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17413493



Internal ID22471363
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:145260217..145261225hg38UCSC Ensembl
chr4:146181369..146182377hg19UCSC Ensembl
Cytoband4q31.21
Allele length
AssemblyAllele length
hg381009
hg191009
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5900708
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17413493
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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