A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18058367



Internal ID20625407
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:225621282..225621591hg38UCSC Ensembl
chr1:225808984..225809293hg19UCSC Ensembl
Cytoband1q42.12
Allele length
AssemblyAllele length
hg38310
hg19310
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6326103
Supporting Variants
Samples
Known GenesENAH
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18058367
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00031


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