A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5869051



Internal ID22643986
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:43583256..43622188hg38UCSC Ensembl
chr21:45003137..45042069hg19UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg3838933
hg1938933
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17480909
Samples
Known GenesHSF2BP, MIR6070
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5869051
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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