A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5956817



Internal ID22731973
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:29653727..29653785hg38UCSC Ensembl
chr21:31026047..31026105hg19UCSC Ensembl
Cytoband21q21.3
Allele length
AssemblyAllele length
hg3859
hg1959
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17398323
Samples
Known GenesGRIK1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5956817
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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