A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6551674



Internal ID20924805
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:44498802..44500024hg38UCSC Ensembl
chr21:45918685..45919907hg19UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg381223
hg191223
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18073304
Samples
Known GenesTSPEAR
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6551674
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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