A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6546051



Internal ID20919271
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:44035256..44035620hg38UCSC Ensembl
chr21:45455137..45455501hg19UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg38365
hg19365
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18073271
Samples
Known GenesTRAPPC10
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6546051
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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