A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17545621



Internal ID21869976
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:2366324..2369688hg38UCSC Ensembl
chr4:2368051..2371415hg19UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg383365
hg193365
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5996746
Supporting Variants
Samples
Known GenesZFYVE28
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17545621
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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