A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17416929



Internal ID22474799
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:2373224..2373295hg38UCSC Ensembl
chr4:2374951..2375022hg19UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg3872
hg1972
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5901889
Supporting Variants
Samples
Known GenesZFYVE28
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17416929
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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