A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5949920



Internal ID22725359
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:36327322..36327842hg38UCSC Ensembl
chr21:37699620..37700140hg19UCSC Ensembl
Cytoband21q22.12
Allele length
AssemblyAllele length
hg38521
hg19521
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17401865
Samples
Known GenesMORC3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5949920
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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