A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5845504



Internal ID22620439
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:41595431..41596665hg38UCSC Ensembl
chr6:41563169..41564403hg19UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg381235
hg191235
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17505765
Samples
Known GenesFOXP4
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5845504
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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