A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16286396



Internal ID20495614
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:40609060..40609652hg38UCSC Ensembl
chr21:41980987..41981579hg19UCSC Ensembl
Cytoband21q22.2
Allele length
AssemblyAllele length
hg38593
hg19593
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4761125
Supporting Variants
Samples
Known GenesDSCAM
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16286396
Frequency
Sample Size25
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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