A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17411418



Internal ID22469288
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:40483707..40490330hg38UCSC Ensembl
chr3:40525198..40531821hg19UCSC Ensembl
Cytoband3p22.1
Allele length
AssemblyAllele length
hg386624
hg196624
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5891089
Supporting Variants
Samples
Known GenesZNF619
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17411418
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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