A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4768218



Internal ID20544078
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:40027062..40034987hg38UCSC Ensembl
chr21:41398989..41406914hg19UCSC Ensembl
Cytoband21q22.2
Allele length
AssemblyAllele length
hg387926
hg197926
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16289220
Samples
Known GenesDSCAM
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4768218
Frequency
Sample Size25
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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