A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6550593



Internal ID20923732
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:41854850..41855591hg38UCSC Ensembl
chr21:43274959..43275700hg19UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg38742
hg19742
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18071556
Samples
Known GenesPRDM15
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6550593
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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