A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16264034



Internal ID20473252
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:121055498..121055649hg38UCSC Ensembl
chr4:121976653..121976804hg19UCSC Ensembl
Cytoband4q27
Allele length
AssemblyAllele length
hg38152
hg19152
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4750143
Supporting Variants
Samples
Known GenesNDNF
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16264034
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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