A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6552792



Internal ID20925919
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:17789801..17794000hg38UCSC Ensembl
chr21:19162118..19166317hg19UCSC Ensembl
Cytoband21q21.1
Allele length
AssemblyAllele length
hg384200
hg194200
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18069454
Samples
Known GenesC21orf91, C21orf91-OT1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6552792
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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