A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5868743



Internal ID22643678
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:33163107..33166571hg38UCSC Ensembl
chr21:34535413..34538877hg19UCSC Ensembl
Cytoband21q22.11
Allele length
AssemblyAllele length
hg383465
hg193465
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17480306
Samples
Known GenesC21orf54
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5868743
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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