A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17418320



Internal ID22476190
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:3308999..3309715hg38UCSC Ensembl
chr4:3310726..3311442hg19UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg38717
hg19717
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5897225
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17418320
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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