A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18065336



Internal ID20632376
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:96487131..96489961hg38UCSC Ensembl
chr1:96952687..96955517hg19UCSC Ensembl
Cytoband1p21.3
Allele length
AssemblyAllele length
hg382831
hg192831
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6332198
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18065336
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00028


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