A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17547762



Internal ID21872117
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:121055496..121055648hg38UCSC Ensembl
chr4:121976651..121976803hg19UCSC Ensembl
Cytoband4q27
Allele length
AssemblyAllele length
hg38153
hg19153
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5994936
Supporting Variants
Samples
Known GenesNDNF
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17547762
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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