A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18072459



Internal ID20639499
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:42232238..42236425hg38UCSC Ensembl
chr21:43652348..43656535hg19UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg384188
hg194188
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6536420
Supporting Variants
Samples
Known GenesABCG1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18072459
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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