A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3937237



Internal ID21357307
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:42108880..42108880hg38UCSC Ensembl
chr21:43528990..43528990hg19UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg38377
hg19377
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15187299
SamplesHG002
Known GenesUMODL1
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3937237
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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