A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16934096



Internal ID23464
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:71199827..71201295hg38UCSC Ensembl
chr3:71248978..71250446hg19UCSC Ensembl
Cytoband3p13
Allele length
AssemblyAllele length
hg381469
hg191469
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5451341
Supporting Variants
Samples
Known GenesFOXP1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16934096
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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