A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17546384



Internal ID21870739
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:120421179..120421372hg38UCSC Ensembl
chr4:121342334..121342527hg19UCSC Ensembl
Cytoband4q27
Allele length
AssemblyAllele length
hg38194
hg19194
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5994885
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17546384
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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