A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17553922



Internal ID21878277
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:121237934..121237989hg38UCSC Ensembl
chr4:122159089..122159144hg19UCSC Ensembl
Cytoband4q27
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5994890
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17553922
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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