A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17480282



Internal ID22538185
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:29763869..29766877hg38UCSC Ensembl
chr21:31136188..31139196hg19UCSC Ensembl
Cytoband21q21.3
Allele length
AssemblyAllele length
hg383009
hg193009
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5885040
Supporting Variants
Samples
Known GenesGRIK1, GRIK1-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17480282
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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