A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6547250



Internal ID20920452
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:19073701..19075800hg38UCSC Ensembl
chr21:20446020..20448119hg19UCSC Ensembl
Cytoband21q21.1
Allele length
AssemblyAllele length
hg382100
hg192100
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18205908
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6547250
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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