A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18073261



Internal ID20640301
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:43940275..43940911hg38UCSC Ensembl
chr21:45360156..45360792hg19UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg38637
hg19637
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6554255
Supporting Variants
Samples
Known GenesAGPAT3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18073261
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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