A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17557224



Internal ID21881579
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:192602740..192671806hg38UCSC Ensembl
chr3:192320529..192389595hg19UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg3869067
hg1969067
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5992458
Supporting Variants
Samples
Known GenesFGF12
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17557224
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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