A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6548625



Internal ID20921809
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:44976301..44997400hg38UCSC Ensembl
chr21:46396216..46417314hg19UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg3821100
hg1921099
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18204157
Samples
Known GenesFAM207A, LINC00163
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6548625
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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