A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17545491



Internal ID21869846
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:196833466..196852686hg38UCSC Ensembl
chr3:196560337..196579557hg19UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg3819221
hg1919221
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5993003
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17545491
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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