A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4767555



Internal ID20543415
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:40023712..40038339hg38UCSC Ensembl
chr21:41395639..41410266hg19UCSC Ensembl
Cytoband21q22.2
Allele length
AssemblyAllele length
hg3814628
hg1914628
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16277737
Samples
Known GenesDSCAM
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4767555
Frequency
Sample Size25
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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