A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5874607



Internal ID22649560
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:32293667..32296666hg38UCSC Ensembl
chr21:33665978..33668977hg19UCSC Ensembl
Cytoband21q22.11
Allele length
AssemblyAllele length
hg383000
hg193000
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17488497
Samples
Known GenesMRAP
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5874607
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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