A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5870273



Internal ID22645209
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:29917544..29956283hg38UCSC Ensembl
chr21:31289862..31328601hg19UCSC Ensembl
Cytoband21q21.3
Allele length
AssemblyAllele length
hg3838740
hg1938740
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17488484
Samples
Known GenesGRIK1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5870273
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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