A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5864489



Internal ID22639424
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:43890335..43901681hg38UCSC Ensembl
chr11:43911885..43923231hg19UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg3811347
hg1911347
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17463429
Samples
Known GenesALKBH3, SEC14L1P1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5864489
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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