A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6542635



Internal ID20915893
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:18223723..18224478hg38UCSC Ensembl
chr21:19596040..19596795hg19UCSC Ensembl
Cytoband21q21.1
Allele length
AssemblyAllele length
hg38756
hg19756
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18069499
Samples
Known GenesCHODL
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6542635
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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