A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6553586



Internal ID20926697
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:26649079..26739138hg38UCSC Ensembl
chr21:28021398..28111457hg19UCSC Ensembl
Cytoband21q21.3
Allele length
AssemblyAllele length
hg3890060
hg1990060
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18206023
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6553586
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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