A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18065771



Internal ID20632811
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:97929004..97929447hg38UCSC Ensembl
chr1:98394560..98395003hg19UCSC Ensembl
Cytoband1p21.3
Allele length
AssemblyAllele length
hg38444
hg19444
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6315720
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18065771
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00142


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