A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6539274



Internal ID20912575
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:29551401..29554500hg38UCSC Ensembl
chr21:30923722..30926821hg19UCSC Ensembl
Cytoband21q21.3
Allele length
AssemblyAllele length
hg383100
hg193100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18072031
Samples
Known GenesGRIK1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6539274
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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