A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17413107



Internal ID22470977
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:3901425..4174137hg38UCSC Ensembl
chr4:3903152..4175864hg19UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg38272713
hg19272713
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5905330
Supporting Variants
Samples
Known GenesFAM86EP
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17413107
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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