A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6549449



Internal ID20922610
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:26864834..28052292hg38UCSC Ensembl
chr21:28237153..29424611hg19UCSC Ensembl
Cytoband21q21.3
Allele length
AssemblyAllele length
hg381187459
hg191187459
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18206024
Samples
Known GenesADAMTS5, LINC00113, LINC00314, MIR4759, MIR5009
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6549449
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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