A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6551701



Internal ID20924833
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:43854253..43860397hg38UCSC Ensembl
chr21:45274134..45280278hg19UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg386145
hg196145
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18072025
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6551701
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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