A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4750143



Internal ID20526179
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 StatusM
Merged Variants
Supporting Variantsnssv16264034
Samples
Known GenesNDNF
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4750143
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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