A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6069328



Internal ID21978561
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:71158151..71158151hg38UCSC Ensembl
chr3:71207302..71207302hg19UCSC Ensembl
Cytoband3p13
Allele length
AssemblyAllele length
hg38158
hg19158
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17553216
Samples
Known GenesFOXP1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6069328
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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