A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6550970



Internal ID20924113
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:16389803..16417454hg38UCSC Ensembl
chr21:17762123..17789774hg19UCSC Ensembl
Cytoband21q21.1
Allele length
AssemblyAllele length
hg3827652
hg1927652
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18203787
Samples
Known GenesLINC00478
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6550970
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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