A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18059568



Internal ID20626608
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:243559810..243560290hg38UCSC Ensembl
chr1:243723112..243723592hg19UCSC Ensembl
Cytoband1q44
Allele length
AssemblyAllele length
hg38481
hg19481
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6320917
Supporting Variants
Samples
Known GenesAKT3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18059568
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00155


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