A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17427418



Internal ID22485288
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:32666572..32669831hg38UCSC Ensembl
chr4:32668194..32671453hg19UCSC Ensembl
Cytoband4p15.1
Allele length
AssemblyAllele length
hg383260
hg193260
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5903402
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17427418
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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