A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5996865



Internal ID21906208
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:2061437..2062230hg38UCSC Ensembl
chr4:2063164..2063957hg19UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg38794
hg19794
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17548387
Samples
Known GenesNAT8L
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5996865
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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