A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6546618



Internal ID20919828
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:33959642..33962333hg38UCSC Ensembl
chr21:35331945..35334635hg19UCSC Ensembl
Cytoband21q22.11
Allele length
AssemblyAllele length
hg382692
hg192691
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18072000
Samples
Known GenesLINC00649
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6546618
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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