A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5867936



Internal ID22642871
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:42182975..42187178hg38UCSC Ensembl
chr1:42648646..42652849hg19UCSC Ensembl
Cytoband1p34.2
Allele length
AssemblyAllele length
hg384204
hg194204
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17382144
Samples
Known GenesFOXJ3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5867936
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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