A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6546359



Internal ID20919577
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:44020948..44023181hg38UCSC Ensembl
chr21:45440829..45443062hg19UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg382234
hg192234
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18073269
Samples
Known GenesTRAPPC10
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6546359
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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