A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17555493



Internal ID21879848
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:71280431..71280588hg38UCSC Ensembl
chr3:71329582..71329739hg19UCSC Ensembl
Cytoband3p13
Allele length
AssemblyAllele length
hg38158
hg19158
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5993719
Supporting Variants
Samples
Known GenesFOXP1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17555493
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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