A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6541804



Internal ID20915072
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:32603930..32605666hg38UCSC Ensembl
chr21:33976240..33977976hg19UCSC Ensembl
Cytoband21q22.11
Allele length
AssemblyAllele length
hg381737
hg191737
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18071940
Samples
Known GenesC21orf59
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6541804
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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