A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5885040



Internal ID22660024
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:29763869..29766877hg38UCSC Ensembl
chr21:31136188..31139196hg19UCSC Ensembl
Cytoband21q21.3
Allele length
AssemblyAllele length
hg383009
hg193009
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17480282
Samples
Known GenesGRIK1, GRIK1-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5885040
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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