A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5836781



Internal ID22611716
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:71282136..71283204hg38UCSC Ensembl
chr3:71331287..71332355hg19UCSC Ensembl
Cytoband3p13
Allele length
AssemblyAllele length
hg381069
hg191069
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17494725
Samples
Known GenesFOXP1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5836781
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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