A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17544925



Internal ID21869280
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:105898290..105898347hg38UCSC Ensembl
chr4:106819447..106819504hg19UCSC Ensembl
Cytoband4q24
Allele length
AssemblyAllele length
hg3858
hg1958
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5994653
Supporting Variants
Samples
Known GenesNPNT
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17544925
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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