A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18073358



Internal ID20640398
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:45111065..45122211hg38UCSC Ensembl
chr21:46530980..46542126hg19UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg3811147
hg1911147
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6547479
Supporting Variants
Samples
Known GenesADARB1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18073358
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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