A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6554129



Internal ID20927236
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:20992059..21021411hg38UCSC Ensembl
chr21:22364377..22393728hg19UCSC Ensembl
Cytoband21q21.1
Allele length
AssemblyAllele length
hg3829353
hg1929352
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18205936
Samples
Known GenesNCAM2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6554129
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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