A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5836753



Internal ID22611688
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:71345719..71351559hg38UCSC Ensembl
chr3:71394870..71400710hg19UCSC Ensembl
Cytoband3p13
Allele length
AssemblyAllele length
hg385841
hg195841
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17494727
Samples
Known GenesFOXP1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5836753
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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