A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6547719



Internal ID20920920
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:17791601..17792154hg38UCSC Ensembl
chr21:19163918..19164471hg19UCSC Ensembl
Cytoband21q21.1
Allele length
AssemblyAllele length
hg38554
hg19554
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18069455
Samples
Known GenesC21orf91, C21orf91-OT1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6547719
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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