A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6067443



Internal ID21976676
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:71113733..71113733hg38UCSC Ensembl
chr3:71162884..71162884hg19UCSC Ensembl
Cytoband3p13
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17548018
Samples
Known GenesFOXP1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6067443
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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