A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5867690



Internal ID22642625
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:46533889..46536488hg38UCSC Ensembl
chr21:47953802..47956401hg19UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg382600
hg192600
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17488949
Samples
Known GenesDIP2A
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5867690
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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