A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17543631



Internal ID21867986
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:71115492..71115561hg38UCSC Ensembl
chr3:71164643..71164712hg19UCSC Ensembl
Cytoband3p13
Allele length
AssemblyAllele length
hg3870
hg1970
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5993922
Supporting Variants
Samples
Known GenesFOXP1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17543631
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer