A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17547773



Internal ID21872128
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:71399161..71400663hg38UCSC Ensembl
chr3:71448312..71449814hg19UCSC Ensembl
Cytoband3p13
Allele length
AssemblyAllele length
hg381503
hg191503
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5993925
Supporting Variants
Samples
Known GenesFOXP1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17547773
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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