A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17979284



Internal ID20546324
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:25157582..25158009hg38UCSC Ensembl
chr10:25446511..25446938hg19UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg38428
hg19428
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6436461
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17979284
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00446


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