A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5874446



Internal ID22649398
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:36010756..36019684hg38UCSC Ensembl
chr21:37383054..37391982hg19UCSC Ensembl
Cytoband21q22.12
Allele length
AssemblyAllele length
hg388929
hg198929
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17488512
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5874446
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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