A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6553607



Internal ID20926718
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:22045350..22189219hg38UCSC Ensembl
chr21:23417669..23561538hg19UCSC Ensembl
Cytoband21q21.1
Allele length
AssemblyAllele length
hg38143870
hg19143870
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18069975
Samples
Known GenesLINC00308
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6553607
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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