A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18065066



Internal ID20632106
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:84533689..84534322hg38UCSC Ensembl
chr1:84999372..85000005hg19UCSC Ensembl
Cytoband1p22.3
Allele length
AssemblyAllele length
hg38634
hg19634
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6333388
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18065066
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00057


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