A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5830721



Internal ID22605656
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:63540683..63549661hg38UCSC Ensembl
chr1:64006354..64015332hg19UCSC Ensembl
Cytoband1p31.3
Allele length
AssemblyAllele length
hg388979
hg198979
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17481118
Samples
Known GenesDLEU2L, EFCAB7
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5830721
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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